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Japanese Journal of Genetic Counseling
Volume 32, Issue 2 / 2011
English Article Japanese Article
- Please note that metadata of J-type articlesare generated by machine-translation and the original texts are written in Japanese.
Overview Tsutomu Nobori 1, 2, Masayoshi Tsutsumi 2, 3 Japanese Journal of Genetic Counseling 32(2): 20-20, 2011. |
Establishment of the highly precise genotype in the Japanese of the Pharmacokinetics-related gene cluster to investigate the difference that is S1-1 drug-responsive and genome sequencing method Akihiro Sekine 1, Takuya Kitamoto 1, Aya Kitamoto 1, Mizusawa spirit ear 2, Satoshi Teranishi 2, Kikuko Hotta 1, Kenji Ueshima 1, 小杉眞司 3, Kazuwa Nakao 1 Japanese Journal of Genetic Counseling 32(2): 20-21, 2011. |
The action present conditions and problem of PGx in the S1-2 drug industry Liu world ball Japanese Journal of Genetic Counseling 32(2): 21-22, 2011. |
The present conditions and problem of the PGx study in S1-3 cancer clinical trials Kazuto Nishio Japanese Journal of Genetic Counseling 32(2): 22-22, 2011. |
About correspondence to PGx in the pharmaceutical administration of the S1-4 our country Shinji Miyake Japanese Journal of Genetic Counseling 32(2): 22-22, 2011. |
Overview Masakazu Toi Japanese Journal of Genetic Counseling 32(2): 23-23, 2011. |
- clinical from present conditions and fine-view - basics of S2-1 BRCA1/2 study Yoshio Miki 1, 2 Japanese Journal of Genetic Counseling 32(2): 23-24, 2011. |
The internal and external situation about the application of the S2-2 BRCA genetic screening Chikashi Ishioka Japanese Journal of Genetic Counseling 32(2): 24-24, 2011. |
Clinic of S2-3 family-related breast cancer Tadashi Nomizu Japanese Journal of Genetic Counseling 32(2): 24-25, 2011. |
The present conditions and problem of Triple negative breast cancer treatment in the S2-4 our country Shin Masuda three Japanese Journal of Genetic Counseling 32(2): 25-25, 2011. |
Mechanism of action of the PARP inhibitor as a function and the anticancer drug of S2-5 PARP Gain valley Mitsuko Japanese Journal of Genetic Counseling 32(2): 26-26, 2011. |
Clinical development of the S2-6 PARP inhibitor Hiroshi Minami sincerity Japanese Journal of Genetic Counseling 32(2): 26-26, 2011. |
Overview Hideaki Sawai Japanese Journal of Genetic Counseling 32(2): 27-27, 2011. |
A diagnosis and genetic background of the S3-1 fetuses systemic bone disease Hideaki Sawai Japanese Journal of Genetic Counseling 32(2): 27-27, 2011. |
Fetal hydrocephalus by the S3-2 genetic factor Asami Yamazaki 1, Kanemura rice Expo 1, Masahiro Nonaka 1, Husband Ritsuko 2 Japanese Journal of Genetic Counseling 32(2): 28-28, 2011. |
Genetic problem to be found in pregnancy by the S3-3 reproductive medicine Kiyonori Miura, Hideaki Masuzaki Japanese Journal of Genetic Counseling 32(2): 29-29, 2011. |
Across S3-4 genetics to epigenetic epigenetic - of - perinatal period Kenichiro Hata Japanese Journal of Genetic Counseling 32(2): 29-29, 2011. |
Overview Numabe Hironao 1, West Takahiro Komori 2 Japanese Journal of Genetic Counseling 32(2): 30-30, 2011. |
Base maintenance of the S4-1 primary immunodeficiency disease study 小原收 1, 2 Japanese Journal of Genetic Counseling 32(2): 30-30, 2011. |
Gene practice in the S4-2 T cell line immunopathy Tomohiro Morio Japanese Journal of Genetic Counseling 32(2): 31-31, 2011. |
Clinical genetics in the S4-3 antibody production deficiency Gold and Hirokazu Japanese Journal of Genetic Counseling 32(2): 31-32, 2011. |
About gene diagnosis in the self-inflammatory disease in S4-4 Japan West Takahiro Komori Japanese Journal of Genetic Counseling 32(2): 32-32, 2011. |
Overview Yasuko Yamauchi 1, Hiromi Murakami 5, Noriko Tanabe 2, Kazumi Omachi 3, Hatakeyama future 4, Minoru Kaneko Motoko 4, Yuki Sato 5 Japanese Journal of Genetic Counseling 32(2): 33-33, 2011. |
S5-1 authorized counselor heredity - training, qualification, tissue, global image - Yasuko Yamauchi Japanese Journal of Genetic Counseling 32(2): 33-34, 2011. |
For process and the future of counselor S5-2 authorized heredity ethic general plan - development - Hiromi Murakami, 小杉眞司 Japanese Journal of Genetic Counseling 32(2): 34-35, 2011. |
The relation of the authorized heredity counselor in the practice system establishment of familial tumor in the S5-3 Shikoku cancer center and the future prospects Shozo Osumi, Valley water Masato, Yoshiro Kubo, Blue matter Kenjiro, Moat Shinichiro, Takashi Matsumoto, Yuko Shiroyama, Mina Takahashi, Haruna Masuda, Kaori Tadokoro Japanese Journal of Genetic Counseling 32(2): 35-35, 2011. |
Role of the heredity counselor in the S5-4 cancer center Haruna Masuda Japanese Journal of Genetic Counseling 32(2): 36-36, 2011. |
A comprehensive medicine system and genetic counseling for the S5-5 rare hereditary circulatory disease Yuko Morizaki 1, 2, Akiko Ono 1, 3, Takayuki Morizaki 1, 2, 4 Japanese Journal of Genetic Counseling 32(2): 36-37, 2011. |
Activity of the authorized heredity counselor in the extensive medical research center specialized in S5-6 circulatory disease Akiko Ono 1, 2, Yuko Morizaki 1, 3, Takayuki Morizaki 1, 3, 4 Japanese Journal of Genetic Counseling 32(2): 37-38, 2011. |
Stand on the action of - laboratory study center and the duties of the counselor authorization heredity from the situation of the authorized heredity counselor working in S5-7 laboratory study center Mikiko Izumi 1, Kaneko view incense 1, Gondo Enkyu era 1, 2 Japanese Journal of Genetic Counseling 32(2): 38-38, 2011. |
S6 The current state of prenatal screening and testing in the United States and the role of genetic counselors at Genzyme Genetics 小野塚香織 Japanese Journal of Genetic Counseling 32(2): 39-39, 2011. |
Overview 櫻井晃洋 1, Shinichi Suzuki 2 Japanese Journal of Genetic Counseling 32(2): 40-40, 2011. |
It is result and the future to this S7-1 multiple endocrine neoplasia symptom study consortium 櫻井晃洋 Japanese Journal of Genetic Counseling 32(2): 41-41, 2011. |
The present conditions of the gene diagnosis and new therapy for MEN in the S7-2 country Shinnya Uchino Japanese Journal of Genetic Counseling 32(2): 41-41, 2011. |
About making of the practice guideline in the S7-3 multiple endocrine neoplasia symptom Shinichi Suzuki Japanese Journal of Genetic Counseling 32(2): 42-42, 2011. |
S7-4 Advocacy group for patients with MEN and their family members "Mukuroji-no-Kai" むくろじの会 Japanese Journal of Genetic Counseling 32(2): 42-42, 2011. |
S7-5 Patients supporting patients with multiple endocrine neoplasia Jo Grey Japanese Journal of Genetic Counseling 32(2): 43-43, 2011. |
Distortion and pathogenesis mechanism of embryology - morphogenesis for T medical genetics Kohei Shiota Japanese Journal of Genetic Counseling 32(2): 44-44, 2011. |
Overview 小杉眞司 Japanese Journal of Genetic Counseling 32(2): 45-45, 2011. |
Construction of "the study governance" in the S8-1 genomics Tetsuya Shirai 1, Mitsunari Kotobuki product 1, Kazuto Kato 1, 2, 3 Japanese Journal of Genetic Counseling 32(2): 46-46, 2011. |
It is a policy and the ethic in the design of the sample collection of business S8-2 bio banking Toru Masui Japanese Journal of Genetic Counseling 32(2): 47-47, 2011. |
The present conditions and problem of the issue of S8-3 rare intractable disease Jiro Koizumi 1, 2 Japanese Journal of Genetic Counseling 32(2): 47-47, 2011. |
The heredity teaching materials to use in S8-4 Elementary School Naoko Nakagawa 1, Numabe Hironao 2, 小杉眞司 2 Japanese Journal of Genetic Counseling 32(2): 48-48, 2011. |
Overview Mitsuru Emi 1, Takeo Kato 2 Japanese Journal of Genetic Counseling 32(2): 49-49, 2011. |
It is an approach from CNV analysis disease for S9-1 adulthood Mitsuru Emi 1, 2 Japanese Journal of Genetic Counseling 32(2): 49-49, 2011. |
Copy number change of the isopentenyl diphosphate isomerase gene region in S9-2 isolated amyotrophic lateral sclerosis Takeo Kato 1, Mitsuru Emi 1, 2, Hidenori Sato 1, 2, Toshima solstice 3, Sofue former 4, Kenichi Matsubara 2 Japanese Journal of Genetic Counseling 32(2): 50-50, 2011. |
High-frequency genome deletion in patients with young onset type II diabetes mellitus by all S9-3 genome CNV analysis Hiroshi Kudo kernel, Tetsuya Yamada, Hideki Katagiri, Yoshitomo Oka Japanese Journal of Genetic Counseling 32(2): 50-51, 2011. |
CNV analysis of S9-4 osteoporosis Tomohiko Urano 1, 2, Masataka Shiraki 3, Yasuyoshi Ouchi 2, Satoshi Inoue 1, 2 Japanese Journal of Genetic Counseling 32(2): 51-51, 2011. |
High-frequency copy number deletion in the chromosome subtelomere region in patients with S9-5 isolated Parkinson's disease Hidenori Sato, Mitsuru Emi, Wild young Shigeki, Manabu Wada, 川並透, Takeo Kato Japanese Journal of Genetic Counseling 32(2): 52-52, 2011. |
CNV analysis by the S9-6 MLPA method Gondo Enkyu era 1, 2, Arata Takahashi 1, Joji Kobayashi 1, Circle shallows Hideaki 1 Japanese Journal of Genetic Counseling 32(2): 52-52, 2011. |
ABC of breast cancer, ovarian cancer (HBOC) hereditary for L1 Gondo Enkyu era 1, 2, Kaneko view incense 1, Mikiko Izumi 1 Japanese Journal of Genetic Counseling 32(2): 53-53, 2011. |
The prospects to the introduction of the genetic analysis technology that is the latest for L2 and diagnosis application Sugimoto light Japanese Journal of Genetic Counseling 32(2): 53-53, 2011. |
The future prospects of the L3 DNA microarray testing Satoshi Tashiro, Yoko Ikeda, Masakazu Nakano, Natsue Omi, Kazuhiko Mori, Shigeru Kinoshita Japanese Journal of Genetic Counseling 32(2): 54-54, 2011. |
The present conditions of the use of microarrays in the L4 heredity medical care Kenjiro Kozaki Japanese Journal of Genetic Counseling 32(2): 55-55, 2011. |
Analysis of 27 cases to lack in genetic testing and genetic counseling - family history of spinocerebellar degeneration in the O-01 Chiba University Hospital 澤井摂 1, 2, Emi Utsuno 2, Number of Kanai light 3, Kenichi Sato 2, Takashi Ishige 2, Itoga 2, Sakae, Motoi Nishimura 1, 2, Kazuyuki Matsushita 1, 2, Satoshi Kuwahara 3, Fumio Nomura 1, 2 Japanese Journal of Genetic Counseling 32(2): 56-56, 2011. |
Report of the diagnosis experience before hereditary neurodegenerative disease onset in the O-02 senior Pope Kengo Uemura 1, Numabe Hironao 2, Hiroshi Yamashita 1, Takayuki Kondo 1, Ai Tanigaki 1, Hinokigawa Rii 1, 浦尾充子 2, Tomiwa Kiyotaka 3, Ryoho Takahashi 1 Japanese Journal of Genetic Counseling 32(2): 56-56, 2011. |
Examination of the prenatal diagnosis of O-03 myelopathic muscular atrophy (SMA) Mari Urano, Soraku existence Noriko, Kayoko Saito Japanese Journal of Genetic Counseling 32(2): 56-56, 2011. |
Genetic counseling of the mitochondrial illness in O-04 Kunitachi mind, the nerve medical research center Yukiko Sato, Yayoi Ikegami, Yuichi Goto Japanese Journal of Genetic Counseling 32(2): 57-57, 2011. |
Gene diagnosis of Unverricht-Lundborg disease in our O-05 institution Takayuki Kondo, Hiroshi Yamashita, Kengo Uemura, Jun Kawamata, Ai Tanigaki, Hinokigawa Rii, Katsuya Kobayashi, Takeshi Hitomi sentence, Matsumoto law of nature device, Akio Ikeda, Ryoho Takahashi Japanese Journal of Genetic Counseling 32(2): 57-57, 2011. |
Genetic counseling of O-06 autistic spectrum disorder Hiroko Taniai 1, 2, Satoshi Washimi 1, 3, Bell Nobuhiro Mori 1 Japanese Journal of Genetic Counseling 32(2): 57-57, 2011. |
Seriously ill joint type Ehlers-Danlos syndrome following course progressive rapidly with the onset, pervasive developmental disorder with the spasticity of O-07 lower limbs Tomoki Kosho 1, Yoko Narumi 1, Seki Island Yoshiki 1, Asako Mizuuchi 1, Hiromi Yamashita 1, Mariko Tamai 1, 櫻井晃洋 1, Jun Watanabe 2, Yoshimitsu Fukushima 1 Japanese Journal of Genetic Counseling 32(2): 58-58, 2011. |
Step of O-08 Fukuoka clinic heredity meeting for the study ten years Masanobu Ogawa 1, Yasuyuki Hasuo 1, Saito relation way 2, 當時久保正之 2, Yoshizato Toshiyuki 3, Kumiko Okubo 3, Makiko Yuki 3, Hisashi Nakagawa 3, Kenji Ihara 4, Kanako Ishii 4, Matsushita holy liquor 4, Sanae Numata 5, Harada なをみ 5, Sayuri Kishimoto 6, Atsushi Ishii 6, Takahito Inoue 7, Bank sincerity 8, Nobuko Kanai 9 Japanese Journal of Genetic Counseling 32(2): 58-58, 2011. |
The present conditions of the genetic counseling in the O-09 Osaka Prefectural maternal and child health comprehensive medical care center Akimaru Noriko 1, Keiko Matsuda 1, 2, Yuko Mishima 1, Atsuko Ikegawa 1, Yuto Yamamoto 1, Nobuhiko Okamoto 1 Japanese Journal of Genetic Counseling 32(2): 58-58, 2011. |
Establishment of the pediatric heredity unit in the O-10 Tama, Tokyo area Hiroshi Kichihashi 1, Shiho Hosokawa 2, Katsumi Tanaka 2, Yutaka Oki straight 3 Japanese Journal of Genetic Counseling 32(2): 59-59, 2011. |
Role of the authorized heredity counselor in the physician-led trial including O-11 pharmacogenomics (PGx) 村島京子1, 2, 3, 大江田知子1, 4, 松井仁美1, 3, 綱本郷子1, 3, 小林恭子1, 3, 脇恭子1, 白石一浩2, 澤田秀幸1, 3, 4 Japanese Journal of Genetic Counseling 32(2): 59-59, 2011. |
Hereditary tumor practice new model system architectural trial in the O-12 area nucleus hospital Chikako Nishida 1, Chieko Tamura 1, 2, Tanakaya Koji 1 Japanese Journal of Genetic Counseling 32(2): 59-59, 2011. |
Experience in the life event of patients with O-13 familial adenomatous polyposis Kaoru Inami 1, Yuko Takeda 1, Tsuyoshi Iwama husband 2 Japanese Journal of Genetic Counseling 32(2): 60-60, 2011. |
It is one patient of the familial adenomatous polyposis (FAP) who had rectal cancer after O-14 large intestine total extirpation, ileoproctostomy for 20 years Yasuhiko Ryu, Akagi reason person, Tetsushi Kinugasa, 石橋生哉, Katsuaki Tanaka, Clay Ichitaro, Yukito Gotanda, Kazuo Shiromizu Japanese Journal of Genetic Counseling 32(2): 60-60, 2011. |
Correlative study on susceptibility to colorectal cancer due to the cause gene of the O-15 familial adenomatous polyposis Sachiko Oishi 1, Urakawa excellent work 1, Hermitage former Michiko 1, Yoshida eyes 1, Nami Shibata 2, Bamboo Taeko Nagatomi 2, Megumi Yoshizawa 2, Okamura peach blossom 2, Chika Yamashita 2, Daichi Murakami 2, Yukio Yokoyama 2, Satoshi Tsuda 3, Takashi Kuno 3, Satoshi Yamano group 3, Masashi Noda 3, Matsubara Nagahide 3, Tomita Hiroshi Shou 3, Junko Tatsumi 1, 2, Kazuo Fujikawa 1, 2, 田村和朗 1, 2 Japanese Journal of Genetic Counseling 32(2): 60-60, 2011. |
Contribution of base excision repair gene MYH in the O-16 colorectal cancer development Takashi Kuno 1, Matsubara Nagahide 1, Satoshi Tsuda 1, Riding ground Akira Tani kernel 1, Hamanaka beauty clothes 1, Daisuke Yamagishi 1, Kiyoshi Tsukamoto 1, Satoshi Yamano group 1, Masashi Noda 1, Megumi Yoshizawa 2, 田村和朗 2, Tomita Hiroshi Shou 1 Japanese Journal of Genetic Counseling 32(2): 61-61, 2011. |
We make practice guidelines on O-17 hereditary colorectal cancer FAP [designated subject] Tsuyoshi Iwama husband 1, Koichi Koizumi 2, Tomita Hiroshi Shou 3, Hideyuki Ishida 1, Satoki Watanabe 4 Japanese Journal of Genetic Counseling 32(2): 61-61, 2011. |
We report the present conditions of the O-18 Lynch's syndrome practice guidelines making [designated subject] Tomita Hiroshi Shou 1, Matsubara Nagahide 1, 田村和朗 2, 赤木究 3, Koichi Koizumi 4, Hideyuki Ishida 5, Satoki Watanabe 6, Tsuyoshi Iwama husband 5 Japanese Journal of Genetic Counseling 32(2): 62-62, 2011. |
Examination of the PMS2 genetic screening for Lynch syndrome gene diagnosis in the O-19 Japanese 川良毅人 1, Yosuke Furui 1, Takashi Fukui 1, Rattan Hiroshi Mori 1, Shiro Yokoyama 1, Gondo Enkyu era 1, Miho Tsunoda 2, 赤木究 2 Japanese Journal of Genetic Counseling 32(2): 62-62, 2011. |
Molecular screening of the Lynch's syndrome using the O-20 colorectal cancer tissue 赤木究 1, Miho Tsunoda 1, Akemi Takahashi 1, Masako Asayama 2, Yoji Nishimura 3, 八岡利昌 3, 山口研成 2, Yoichi Tanaka 3 Japanese Journal of Genetic Counseling 32(2): 63-63, 2011. |
Basic examination about the strategies for treatment of O-21 MSI-positive colorectal cancer Makiko Tahara 1, 2, Futoshi Sato 1, 2, Tsuyoshi Inoue 1, 2, Yasukichi Sugano 1, 2, Shrine storehouse cheap good luck 3, Yoshikazu Yasuda 3 Japanese Journal of Genetic Counseling 32(2): 63-63, 2011. |
Association to develop from O-22 Lower uterine segment(LUS) between uterine cancer and Lynch syndrome Kenta Masuda, 阪埜浩司, 矢野倉恵, Yusuke Kobayashi, Arisa Ueki, Iori Kisu, Hiroyuki Nomura, Akira Hirasawa, 進伸幸, Daisuke Aoki Japanese Journal of Genetic Counseling 32(2): 63-63, 2011. |
The significance of p27 in the O-23 MEN1 mutation in the gene-negative case and the p18 gene from the examination of the high MEN1 case of the grade: Masanobu Yamada 1, Atsushi Ozawa 1, Ryo Taguchi 1, Emi Ishida 1, Masatomo Mori 1, Hiroshi Kaji 2, Tsuneo Imai 3, 櫻井晃洋 4, MEN consortium 1 Japanese Journal of Genetic Counseling 32(2): 64-64, 2011. |
Advanced medical action in the O-24 this hospital Akiko Ito, Shinnya Uchino, Yoko Watanabe, Side shop Shigeko, Neck Fujishige, Shiro Noguchi Japanese Journal of Genetic Counseling 32(2): 64-64, 2011. |
About this country case of the malignant pheochromocytoma due to the O-25 SDHB mutation Kazuhiro Takekoshi 1, Kodama eyes 2, Sanae Midorikawa 3, Sumiko Niisato 1, Kazumasa Isobe 1, Masaya Hoshino 1, Yasushi Kawakami 1, Hideki Tamura 4, Masanobu Yamada 5, Jun Watanabe 6, 櫻井晃洋 7 Japanese Journal of Genetic Counseling 32(2): 64-64, 2011. |
1 case of the bilateral pheochromocytoma that showed new germ cell mutation in O-26 TMEM127 gene Naomi Takeichi 1, Hideki Tamura 1, 2, Toshiko Kano 1, Akira Ishizaki 1, Jin Sugihara 1, Jun Watanabe 3, Taketo Igarashi 4, Azuma Akasu tree 4, Takashi Shimada 3, Kazuo Shimizu 4, Kazumasa Isobe 5, Sumiko Niisato 5, Kazuhiro Takekoshi 5, Shinichi Oikawa 1 Japanese Journal of Genetic Counseling 32(2): 65-65, 2011. |
Clinical condition investigation of O-27 von Hippel Lindau(VHL) disease Ichiro Yamazaki, Kenji Tamura, Ashida Shingo, 執印太郎 Japanese Journal of Genetic Counseling 32(2): 65-65, 2011. |
Action of the genetic information management by the electronic chart in the O-28 Osaka University Hospital Yuki Sato 1, Norio Sakai 1, Takeshi Kanekawa 1, Takanobu Otomo 1, Hamada Yusuke 1, Country prefecture power 1, Komaki Masayasu 1, Yoshizu Kikuko 1, Chikako Nishida 1, Saki Ichimura 1, 上田郁奈代 2, Yasushi Matsumura 2, Noguchi Saburo Sana 1 Japanese Journal of Genetic Counseling 32(2): 66-66, 2011. |
The prospects in process and our country of O-29 Human Variome Project (HVP) Joji Utsunomiya 1, Makoto Tanaka 2 Japanese Journal of Genetic Counseling 32(2): 66-66, 2011. |
It is a function and the enlargement of data MutationView as O-30 unification type LSDB Masashi Otsubo 1, Nobuyoshi Shimizu 2, Shinsei Minoshima 1 Japanese Journal of Genetic Counseling 32(2): 66-66, 2011. |
Calculation algorithmic design and software development of the O-31 inherited disease carriage probability Hiroaki Iijima 1, Shunya Sato 1, Cold water Takashi 1, Numabe Hironao 2, 3 Japanese Journal of Genetic Counseling 32(2): 67-67, 2011. |
Refractory disease conquest study business judging from the side of the O-32 medical genetics Yoshimitsu Fukushima 1, 櫻井晃洋 1, Keiko Wakui 1, Seki Island Yoshiki 1, Tomoki Kosho 1, Yoko Narumi 1, Yuko Morizaki 2, Takayuki Morizaki 2 Japanese Journal of Genetic Counseling 32(2): 67-67, 2011. |
From O-33 recognition, expectation, the attitude survey to misunderstanding - "bio bank Japan" enrolled patients Kaori Muto 1, Maiko Watanabe 1, 洪賢秀 1, Wild inner Takako 2, Mainohara Yoshiko 3, Ayumi Omori 3, Hatakeyama future 3, Jun Watanabe 3, 4, Takashi Shimada 3, 4, South Shiro 3, 5 Japanese Journal of Genetic Counseling 32(2): 67-67, 2011. |
About the second revision of the O-34 "operational guideline of the examination for pharmacogenomics" 堤正好 Japanese Journal of Genetic Counseling 32(2): 68-68, 2011. |
Genetic polymorphism search about onset of severe neutropenia with O-35 docetaxel Your Satoshi Uchiyama 1, Jin Sugano 1, 2, 3, Takeshi Ishitani 4, Aizaki Junko 2, Takako Hamada 2, Juichi Fujii 3, Hideo Matsui 4, Kayoko Saito 1, 2 Japanese Journal of Genetic Counseling 32(2): 68-68, 2011. |
Action to the prenatal diagnosis in the hospital attached to the O-36 Tottori University School of Medicine Shade castle Noriko 1, 2, Kaori Adachi 3, Shuhei Kaneko 4, Yoshito Kikuchi 4, Kosaku Ono 5, Shoko Kondo 5, Masami Togawa 5, Harada 6-saving, Takashi Harada 6, 2, Sakae, Namba 2, 3 Japanese Journal of Genetic Counseling 32(2): 68-68, 2011. |
Examination about 2,000 examination using ammiotic fluid enforcement in the O-37 this hospital Shigeru Sato 1, 2, Kondo vermilion sound 1, 2, Yumiko Goto 1, 2, Takahashi Senka 1, 2, Tadashi Matsumoto 1, 2, 池田仁惠 1, 2, Hiromi Moriya 2, Mitsuko Mizoguchi 2, Katsuhiko Iwasaki 1, Shunichiro Izumi 1, 2 Japanese Journal of Genetic Counseling 32(2): 69-69, 2011. |
The need of the authorized heredity counselor in the reporting of the amniotic fluid chromosomal analysis to O-38 pregnant woman Miyuki Nishiyama 1, 2, Hideaki Sawai 3, 小杉眞司 2 Japanese Journal of Genetic Counseling 32(2): 69-69, 2011. |
2 cases that caused complete chorioamniotic membrane separation after O-39 amniocentesis Hidehiko Miyake 1, 2, Nakanishi one step 1, Yuko Abe 1, Masako Hayashi 1, Your Tadashi Okuda 1, Kawabata Italy Hisano 1, Atsuko Sekiguchi 1, Akito Nakai 1, Jun Watanabe 2, Yuka Oki will 2, Takashi Shimada 2 Japanese Journal of Genetic Counseling 32(2): 69-69, 2011. |
National survey of O-40 Hypermobility Syndrome (EDS joint hypermovable type) [acrocinesia syndrome] Hatakeyama future 1, 2, Jun Watanabe 2, Tomoki Kosho 3, 川目裕 1, Takashi Shimada 2 Japanese Journal of Genetic Counseling 32(2): 70-70, 2011. |
National fact-finding of the O-41 Bardet-Biedl syndrome Makito Hirano 1, Shunei Yamashita 2, Kyoji Ikino 3, Look at Hiroshi Iwahashi; 4, Mitsuru Oishi 5, Toshiyuki Mano 6, 石原立 7, Ichiro Tanaka 8, Keiko Yanagihara 6, Nakamura male product 1, 楠進 9 Japanese Journal of Genetic Counseling 32(2): 70-70, 2011. |
The need of follow-up from heredity practice - perinatal period of O-42 perinatal type hypophosphatasia Jun Watanabe 1, 2, Yumi Suzuki 1, Hanako Sugano 1, 2, Katsuya Mine 3, Takashi Abe 3, Banyar Than Naing2, Toshiyuki Takeshita 3, Hideo Orimo 2, Hideaki Sawai 4, Takashi Shimada 1, 2 Japanese Journal of Genetic Counseling 32(2): 70-70, 2011. |
Congenic - to O-43 fetal gene therapy - severe form hypophosphatasia mouse fetuses Hanako Sugano 1, 2, 3, Jun Watanabe 1, 3, Takashi Shimada 1, 3 Japanese Journal of Genetic Counseling 32(2): 71-71, 2011. |
IL28B gene SNP analysis by O-44 GENECUBE(R) and application to an IFN treatment prognostic value 100, Matsuo sinter 1, Yasusuke Abe 1, Kazushi Sugimoto 1, 2, Junji Nishioka 1, It is 1 of Nakatani, 2, 3, Tsutomu Nobori 1, 2 Japanese Journal of Genetic Counseling 32(2): 71-71, 2011. |
One case of new strain Mycobacterium shinjukuense which caused false-positive by an examination of O-45 tuberculosis mycol. identification Tanaka spring sinter, Haruka Hirose, Miki Takemori, Saori Kida, Hiromi Yonezawa, Eiji Miyajima Japanese Journal of Genetic Counseling 32(2): 71-71, 2011. |
Development of the Pandemic (H1N1) by the O-46 SmartAmp method 2009 virus nucleic acid test for the detection Taiji Kogo 1, 2, Tomohisa Ishikawa 2, 川井雄輝 1, 2, 木村恭将 2, Motoi Kanamori 1, 2, Usui Kengo 2, Yasumasa Mitani 1, 2, Cherry blossom viewing Kenji 2, 相馬崇裕 2, Satomi Saga 2, Yuri Ishizu 2, MORLIGHEM Jean-Etienne2, LEZHAVA Alexander2, Yoshihide Hayashizaki 2 Japanese Journal of Genetic Counseling 32(2): 72-72, 2011. |
Examination of the operational improvement of the O-47 amplifier re-core HPV-related kit Yukiko Miyahara, Toshiaki Miura, Kunihiko Hayashi Japanese Journal of Genetic Counseling 32(2): 72-72, 2011. |
Quality evaluation of the RNA using the O-48 microchip electrophoresis system Mayu Takeda 1, Kuniaki Saito 2, Funato Tadao 1 Japanese Journal of Genetic Counseling 32(2): 72-72, 2011. |
Examination of plasma K-ras mutation in the gene analysis by the O-49 PNA-Clamping sequence method Circle shallows Hideaki 1, Yosuke Furui 1, Takashi Fukui 1, Hiroshi Fujimori 1, Tadaaki Nomoto 1, Shiro Yokoyama 1, Gondo Enkyu era 1, Shozo Miyano 2, Flower Kisaburo Sawa 2 Japanese Journal of Genetic Counseling 32(2): 73-73, 2011. |
Simple and easy detection of the myotonic dystrophy (DM1) CTG amplification repeat using the O-50 Triplet repeat primed PCR (TP-PCR) method Kenichi Sato 1, Itoga 1, Sakae, Takashi Ishige 1, 3, Emi Utsuno 1, 2, 澤井摂 1, 2, 3, Motoi Nishimura 1, 2, 3, Kazuyuki Matsushita 1, 2, 3, Fumio Nomura 1, 2, 3 Japanese Journal of Genetic Counseling 32(2): 73-73, 2011. |
Research and development of clinical somatic gene mutation detection system (Quimple(R)) for O-51 colorectal cancer molecules target effect of treatment predictions Shiro Kitano 1, 2, Wanqing Liu2, Mark Ratain2, Masahiko Amano 1 Japanese Journal of Genetic Counseling 32(2): 73-73, 2011. |
Analysis of the warfarin-related genetic polymorphism by device SNP Analyzer using the O-52 Invader Plus method Kyo Fujita will 1, Ayako Ogasawara 1, 莚田泰誠 2, Jun Watanabe 1, Takashi Shimada 1 Japanese Journal of Genetic Counseling 32(2): 74-74, 2011. |
Search of the life-style related diseases onset risk prediction gene marker which assumed O-53 heredity epidemiology cohort a base Yasuhiko Yoshida 1, Shingo Tsuji 1, 4, 花城薫 1, Asami Kyan 1, 森谷哲浩 1, Kiyonori Iwamoto 1, 顔瑾 1, 長嶺勝 2, Atsushi Sakima 3, Yusuke Ooya 3, 根本靖久 1 Japanese Journal of Genetic Counseling 32(2): 74-74, 2011. |
About a genetic factor of the O-54 gout onset Atsuo Taniguchi, Kazuko Urano, Chieko Sekita, 井上永介, Yumi Ozeki, Naomi Ichikawa, Hisashi Yamanaka Japanese Journal of Genetic Counseling 32(2): 74-74, 2011. |
Association between O-55 IL-5, IL-6, polymorphism and clinical condition prognosis of the autoimmune thyroid disease of the IL-13 gene promotor region Mikio Watanabe 1, Naoya Inoue 1, Asami Morita 1, Keita Tatsumi 2, Hiroshi Hidaka 2, Akamizu Hisafumi 3, Yoshinori Iwatani 1 Japanese Journal of Genetic Counseling 32(2): 75-75, 2011. |
CDH13 genetic polymorphism entangles it in an association between O-56 adiponectin and insulin resistance 田原康玄 1, Ryuichi Kawamoto 2, Katsuhiko Ohara 3, Tetsuro Miki 3 Japanese Journal of Genetic Counseling 32(2): 75-75, 2011. |
The combination of O-57 LDLR gene and PCSK9 mutation in the gene and examination about the LDL-C level Naotaka Ota 1, 2, Mariko Shiha 3, 4, Satoshi Fujiyama beauty 1, 2, Masahiro Fujino 1, 2, Takahiro Sano 1, Noriyuki Iwamoto 3, Hisashi Makino 3, Ichiro Kishimoto 3, 佐野道孝 1, 宮本恵宏 2, 5 Japanese Journal of Genetic Counseling 32(2): 75-75, 2011. |
National fact-finding of the O-58 Costello's syndrome, CFC syndrome and study on clinical condition Yoichi Matsubara 1, Yutaka Abe 1, Tetsuya Niihori 1, Kenji Kurosawa 2, Nobuhiko Okamoto 3, Seiji Mizuno 4, Hirofumi Ohashi 5, 川目裕 6, Tsutomu Ogata 7, Kure Shigeo 8, Shinichi Kuriyama 9, Yoko Aoki 1 Japanese Journal of Genetic Counseling 32(2): 76-76, 2011. |
A prevalence estimate and clinical analysis of the O-59 CHARGE syndrome Yuko Mishima 1, Keiko Matsuda 1, Akimaru Noriko 1, Atsuko Ikegawa 1, Yuto Yamamoto 1, Kenjiro Kozaki 2, Nobuhiko Okamoto 1 Japanese Journal of Genetic Counseling 32(2): 76-76, 2011. |
Clinical picture and genome epigenome analysis of the O-60 this country Beckwith-Wiedemann syndrome 副島英伸, 城崎幸介, 八木ひとみ, 前田寿幸, 大塚泰史, 東元健 Japanese Journal of Genetic Counseling 32(2): 76-76, 2011. |
One case that was complicated with a mesenchymal dysplastic placenta for O-61 Beckwith-Wiedemann syndrome, and presented estrangement for imprinting abnormality of both Junya Miyoshi 1, Isao Sakaguchi 1, Takashi Ohba 1, Hidetaka Kaebuchi 1, Hidenobu Soejima 2, 東元健 2 Japanese Journal of Genetic Counseling 32(2): 77-77, 2011. |
O-62 Three dimensional human embryo "Virtual Human Embryo" using MR image data from Kyoto collecton 高桑徹也1, 山田重人2, 上部千賀子2, 塩田浩平2, 巨瀬勝美3 Japanese Journal of Genetic Counseling 32(2): 77-77, 2011. |
Morphometrical analysis of the emergence of stomach using the O-63 human fetus MRI image Foreign countries Norihito 1, Tetsuya Takakuwa 1, Shigeto Yamada 2, Upper part Chikako 2, Kohei Shiota 2, Katsumi Kose 3 Japanese Journal of Genetic Counseling 32(2): 77-77, 2011. |
Problem for the clinical application of the O-64 array chromosome banding Naoki Harada 1, Takeshi Matsui 1, Kazumasa Saito 1, 霜川修 1, Koichiro Yoshiura 2, Matsumoto direct communication 3, Tatsuro Kondo 4 Japanese Journal of Genetic Counseling 32(2): 78-78, 2011. |
The general adult genome copy number change that was detected by O-65 Cytogenetic Array analysis Keiko Wakui 1, 2, Tomoki Kosho 1, 2, Yoko Narumi 1, 2, Kenji Shimizu 3, Hirofumi Ohashi 3, Yoshimitsu Fukushima 1, 2 Japanese Journal of Genetic Counseling 32(2): 78-78, 2011. |
New characteristic of the disease gene cluster located in the chromosome band border which we pinpointed as O-66 human genome destabilization site Yoshihisa Watanabe, Masato Maekawa Japanese Journal of Genetic Counseling 32(2): 78-78, 2011. |
Report of the preimplantation diagnosis for the habitual abortion due to translocation of chromosome in the O-67 this hospital Ayumi Yamamoto 1, Ai Fukuda product 1, Ryota Kobayashi 1, Yumiko Ueda 1, 樽井幸与 1, Aya Ogaki 1, 五寶秀美 1, Yoshiharu Morimoto 2 Japanese Journal of Genetic Counseling 32(2): 79-79, 2011. |
It is examination about the genetic counseling in the miscarriage case after O-68 infertility treatment Yukiko Katagiri 1, Yusuke Fukuda 2, 3, Sect Akiko 2, 3, Yoichi Matsue 2, 3, Michiko Saegusa 2, 3, Naoki Takeshita 1, Alien from Morita peak 2 Japanese Journal of Genetic Counseling 32(2): 79-79, 2011. |
Decision making of the pregnant woman who had a diagnosis of Trisomy18 during O-69 pregnancy Plum flaming red 1, 2, Hideki Fujita 1, Satoshi Hayashi 3, 左合治彦 3, Kozaki village sinter 1 Japanese Journal of Genetic Counseling 32(2): 79-79, 2011. |
Family system case of the autosomal dominant Aicardi-Goutieres syndrome which led to a diagnosis with O-70 chillblains-like eruption 粟屋智就 1, Kazushi Izawa 1, Junya Abe 1, Takeo Kato 1, 平城徹 2, Heijo Naoko 2, 大嶋勇成 3, West Takahiro Komori 1, Heike Toshio 1 Japanese Journal of Genetic Counseling 32(2): 80-80, 2011. |
Heredity of the O-71 Tokyo Medical College dermatology is foreign Yoshihiko Mitsuhashi, Sakai Noriyasu, Shinki Uchiyama, Tatsuro Maeda, Ryoji Tsuboi Japanese Journal of Genetic Counseling 32(2): 80-80, 2011. |
One case of Bothnia dystrophy of the O-72 Japanese Yoshihiro Hotta 1, Katsuhiro Hosono 1, Nojima 1, Kotobuki in total, 趙洋 1, 2, Hikotani Akiko 1, Kondo peak straight 2, Shinsei Minoshima 3 Japanese Journal of Genetic Counseling 32(2): 80-80, 2011. |
Action to hereditary deafness as the O-73 presenting part medical care 谷口美玲 1, North buttocks Shinichiro 1, Shinichi Usami 2, Juichi Ito 1, 小杉眞司 3 Japanese Journal of Genetic Counseling 32(2): 81-81, 2011. |
Detection of the mutation in the gene of 21 hydroxylase deficiency 132 families in O-74 this country Takeshi Usui 1, Leather Yukiko Shima 2, Tetsuya Tanoe 2, Naruse honor 1, Shimazu chapter 1 Japanese Journal of Genetic Counseling 32(2): 81-81, 2011. |
The fact and problem of the genetic counseling of hemophilia in O-75 Japan Kayo Inoue 1, Mariko Tamai 2, Seki Yukiko 3, Hiroshi Inoue person 4, Yayoi Kitamura 5, Teruyo Nagahama 6, 丹明彦 7, 久地井寿哉 8, Shoot a stone; Izumi 8, Shoko Kakinuma 8, Katsumi Ohira 8, 山本佳世乃 1, 川目裕 1 Japanese Journal of Genetic Counseling 32(2): 81-81, 2011. |
Genetic analysis of the O-76 fanconi anaemia Hermitage former Michiko 1, Emi Uchida 2, Yoshida eyes 1, Junko Tatsumi 1, 3, Takeshi Minami will 1, 3, Kazuo Fujikawa 1, 3, 田村和朗 1, 3, Yabe 4 to watch, Minoru Takada 2 Japanese Journal of Genetic Counseling 32(2): 82-82, 2011. |
It is the analysis of this country 30 families gene diagnosis of O-77 erythropoietic protoporphyria So Nakano 1, Ryoichi Uede 2, Shigeru Kawahara 3, Akira Kawada 3 Japanese Journal of Genetic Counseling 32(2): 82-82, 2011. |
Examination about the attitude survey of the obstetrician for O-78 family-related tumor History of Miura fine weather, Tatsuya Honda, 熊谷晴介, Yoshizaki positive, Akira Fukushima sect, Toru Sugiyama Japanese Journal of Genetic Counseling 32(2): 82-82, 2011. |
Decision making "not to receive" the genetic screening in O-79 family-related tumor 仲田洋美1, 2, 3, 増田春菜1, 岡本陽子2, 堀伸一郎1, 久保義郎1, 白山裕子1, 松本隆1, 青義健二郎1, 大住省三1, 谷水正人1, 金子景香4, 中野芳朗7, 三好康雄5, 冨田尚裕6, 玉置知子3, 7 Japanese Journal of Genetic Counseling 32(2): 83-83, 2011. |
A relation and genetic counseling of familial tumor in the O-80 cancer therapy Masumi Tsunoda 1, 2, Shinichi Suzuki 1, Keiichi Nakano 1, Toshihiko Fukushima 1, Sanae Midorikawa 3, Tadashi Nomizu 4, Seiichi Takenoshita 1 Japanese Journal of Genetic Counseling 32(2): 83-83, 2011. |
In the case of construction - Niigata of the O-81 family-related breast cancer genetic counseling practice system Tatsuyuki Tazawa 1, Kiyoe Goto 1, Jun Toyama 1, 5, Yoko Kuriyama 1, Hideko Sakata 2, 小山諭 2, Nobuaki Sato 3, Muneaki Sano 4, Katsuyoshi Hatakeyama 2, Middle 1, Tabika Japanese Journal of Genetic Counseling 32(2): 83-83, 2011. |
Consensus (from multicenter questionnaire results) of O-82 hereditary, the family-related breast cancer practice 杉江知治 1, Masakazu Toi 1, Light forest path British 2, Chikako Yamauchi 3, Hiroshi Ishiguro 4, Yoshiki Mikami 5, Takashi Okamura kernel 6, Onori Kato 7, Kiyoaki Yamauchi 8, Shun Inamoto 9 Japanese Journal of Genetic Counseling 32(2): 84-84, 2011. |
Examination of the counseling example of the O-83 hereditary breast cancer, ovarian cancer syndrome Maki Hyodo 1, Range Reiko 1, Kase Kei Toshie 1, 家護谷五月 1, Masahiro Ohara 1, Shinya Matsuura 1, 横崎恭之 1, Eizo Hiyama 1, Keiko Hiyama 1, Hirofumi Maruyama 1, Masao Kobayashi 1, 村上茂 2 Japanese Journal of Genetic Counseling 32(2): 84-84, 2011. |
Hope for the genetic screening of patients with O-84 ovarian cancer being performed Nao Kai 1, Mika Miyashita 2, Two Mayumi Itani 2 Japanese Journal of Genetic Counseling 32(2): 84-84, 2011. |
The present conditions of the genetic screening effective time for O-85 hereditary breast cancer, ovarian cancer (HBOC) Seiichiro Nishimura 1, Masami Arai 2, Shiho Hosokawa 2, Taku Iwase person 1 Japanese Journal of Genetic Counseling 32(2): 85-85, 2011. |
Risk assessment of hereditary breast cancer ovarian cancer by the O-86 recursive fractionation Yasukichi Sugano 1, 2, 3, 4, 6, Makishima Keiko 1, Tomota jasmin 1, 2, 3, Kumiko Misu 4, Akira Hirasawa 4, Yuko Takeda 4, 5, Hideko Izumi 5, Teruhiko Yoshida 6, 7 Japanese Journal of Genetic Counseling 32(2): 85-85, 2011. |
Action to the case that had difficulty in diagnosis by O-87 BRCA genetic screening Masami Arai 1, 2, Keiko Taki 1, Yukiko Sugai 2, Miki Komatsu 2, Yuri Sato 1, Seiichiro Nishimura 3, Taku Iwase person 3, Shiro Yokoyama 4, Gondo Enkyu era 4, Yoshio Miki 1, 2 Japanese Journal of Genetic Counseling 32(2): 85-85, 2011. |
Clinicopathologic examination of familial breast cancer in the O-88 our department Hiroyuki Maeda 1, Makoto Yoneta 2, Masako Nakazawa 1, Yasuo Hirono 1, Takanori Goi 1, Atsushi Iida 1, Yutaka Katayama next 1, Hiroshi Ito 3, Imamura enthusiast chapter 4, Akio Yamaguchi 1 Japanese Journal of Genetic Counseling 32(2): 86-86, 2011. |
Clinicopathologic examination of O-89 family-related breast cancer Tortoise Hidekazu Shima 1, Azuma Omura straight 1, Yasuyo Suzuki 1, 九冨五郎 1, Koichi Hirata 1, Tadashi Hasegawa 3 Japanese Journal of Genetic Counseling 32(2): 86-86, 2011. |
Examination of O-90 both sides breast cancer Junko Ishiguro, Tomoyuki Aruga, 山下年成, Eiji Suzuki, Kazumi Horiguchi, Katsumasa Kuroi Japanese Journal of Genetic Counseling 32(2): 86-86, 2011. |
The situation of the inside and outside the country patients association in the P1-01 multiple endocrine neoplasia symptom (MEN) Katai Miyuki 1, 2, 櫻井晃洋 3 Japanese Journal of Genetic Counseling 32(2): 87-87, 2011. |
Collaboration of patients with inherited disease in P1-02 Japan, the family group Takanori Akama 1, 櫻井晃洋 1, Yoshiharu Yokokawa 2, Tetsuo Nomiyama 3, Yoshimitsu Fukushima 1 Japanese Journal of Genetic Counseling 32(2): 87-87, 2011. |
About guidebook making of the inherited disease for the P1-03 patients and the family Hida Miki, Yasuko Yamauchi, 牧優子, Measure field Mitsuo, Yoshikazu Kuroki Japanese Journal of Genetic Counseling 32(2): 87-87, 2011. |
Experience P1-04 heredity medical care and the training about the personnel training in the U.K. Fumio Nomura 1, 澤井摂 1, 2, 3, Maki Kihara 3, 5, Emi Utsuno 2, 3, Kazumi Omachi 3, 4, 葛田衣重 3, 6, Harumi Oguro 3, 7, Hiromi Honma 3, 7, Akira Haneda 3, 4 Japanese Journal of Genetic Counseling 32(2): 88-88, 2011. |
Receive genetic counseling education of P1-05 Kinki University 守井見奈, Michiko in front of a hermitage, Yoshida eyes, Junko Tatsumi, Takeshi Minami will, 田村和朗, Tetsuji Nagao, Kazuo Fujikawa Japanese Journal of Genetic Counseling 32(2): 88-88, 2011. |
Construction of the comprehensive resource of the genetic counseling in P1-06 Japan 市川真臣, Measure field Mitsuo, Yasuko Yamauchi, Yoshikazu Kuroki Japanese Journal of Genetic Counseling 32(2): 88-88, 2011. |
Evaluation as the education tool of the P1-07 heredity drama Keiko Tanaka 1, 櫻井晃洋 2, Yoshimitsu Fukushima 2 Japanese Journal of Genetic Counseling 32(2): 89-89, 2011. |
P1-08 thinks about education of the inherited disease through the impressionistic essay of "1 liter of tear" 松本彬伸 1, Junko Tatsumi 1, 2, 田村和朗 1, 2, Kazuo Fujikawa 1, 2 Japanese Journal of Genetic Counseling 32(2): 89-89, 2011. |
Evaluation second report as the education tool of the comics "genome card" with the P1-09 sound 河村理恵, 櫻井晃洋, 福嶋義光 Japanese Journal of Genetic Counseling 32(2): 89-89, 2011. |
Trial to share P1-10 genetic counseling role playing between distant places by Skype Yuki Kuwahara 1, Junko Tatsumi 1, Sachiko Oishi 1, Urakawa excellent work 1, 松本彬伸 1, Karin Umeda 2, 田村和朗 1, Akira Haneda 2, Kazuo Fujikawa 1 Japanese Journal of Genetic Counseling 32(2): 90-90, 2011. |
P1-11 A Case of Li-Fraumeni syndrome: heterochronous bilateral breast cancer with heterochronous unilateral double 増村京子1, 西村誠一郎1, 新井正美2, 堀井理絵3, 秋山太3, 岩瀬拓士1 Japanese Journal of Genetic Counseling 32(2): 90-90, 2011. |
An example of the PJS families where breast cancer developed in youth though we lacked in a clinical examination of P1-12 Peutz-Jeghers Syndrome(PJS) Hiromi Nakata 1, 2, 3, Haruna Masuda 1, Kaori Tadokoro 1, Moat Shinichiro 1, Yoshiro Kubo 1, Yuko Shiroyama 1, Takashi Matsumoto 1, Blue matter Kenjiro 1, Shozo Osumi 1, Yuki 1 in the chrysanthemum, Saneho Inoue 1, Valley water Masato 1 Japanese Journal of Genetic Counseling 32(2): 90-90, 2011. |
An example of the Lynch syndrome that developed malignant lymphoma and sigmoid colon cancer in P1-13 asynchronism Hiromi Nakata 1, 2, 3, Haruna Masuda 1, Kaori Tadokoro 1, Moat Shinichiro 1, Yoshiro Kubo 1, Yuko Shiroyama 1, Takashi Matsumoto 1, Blue matter Kenjiro 1, Shozo Osumi 1, Yuki 1 in the chrysanthemum, Saneho Inoue 1, Valley water Masato 1 Japanese Journal of Genetic Counseling 32(2): 91-91, 2011. |
Questionary survey about recognition and the examination promotion of the breast cancer risk of the family in patients with P1-14 breast cancer Haruna Masuda 1, Shozo Osumi 1, 2, Kaneko view incense 3, Kaori Tadokoro 1, Hiromi Nakata 1, 4, 5, Sachiko Kiyofuji 2, Mina Takahashi 1, 2, 原文堅 2, 高嶋成輝 2, Onori Takahata 2, Blue matter Kenjiro 1, 2, Valley water Masato 1 Japanese Journal of Genetic Counseling 32(2): 91-91, 2011. |
An example of the bilateral adrenal pheochromocytoma that P1-15 new TMEM127 mutation in the gene was identified Sanae Midorikawa 1, Kazuhiro Takekoshi 2, 佐藤博亮 1, Shinichi Suzuki 3, 笹野公伸 4, Tsuyoshi Watanabe 1 Japanese Journal of Genetic Counseling 32(2): 91-91, 2011. |
Genetic counseling of the patients of the HPPS suspicion due to the SDHB mutation that suffered from P1-16 diagnosis Masumi Tsunoda 1, 2, Shinichi Suzuki 1, Keiichi Nakano 1, Toshihiko Fukushima 1, Sanae Midorikawa 3, Tadashi Nomizu 4, Seiichi Takenoshita 1 Japanese Journal of Genetic Counseling 32(2): 92-92, 2011. |
About problems about the advanced medical use of the P1-17 RET gene diagnosis Neck Fujishige, Shinnya Uchino, Yoko Watanabe, Side shop Shigeko, Akiko Ito, Shiro Noguchi Japanese Journal of Genetic Counseling 32(2): 92-92, 2011. |
By S891A mutation to be found in patients with P1-18 family-related medullary carcinoma of thyroid, the adrenal pheochromocytoma of the unrepresentativeness symptom is presenting symptoms and one case that it was Mizue Oe 1, 2, Hibi eight bundles 3, 小杉眞司 4, 5, Hiroki Kurahashi 1, 2 Japanese Journal of Genetic Counseling 32(2): 92-92, 2011. |
One case of MEN1 who had P1-19 TSHoma 良元紳浩 1, Shinichi Suzuki 1, Chiyo Okochi 1, Left rain Motoki 1, Keiichi Nakano 1, Toshihiko Fukushima 1, Seiichi Takenoshita 2 Japanese Journal of Genetic Counseling 32(2): 93-93, 2011. |
P1-20 multiple endocrine neoplasia symptom study consortium 櫻井晃洋 1, 6, 10, Tsuneo Imai 2, 10, Hiroshi Kaji 3, 10, Masanobu Yamada 4, 10, Atsushi Ozawa 4, 10, Taketo Igarashi 5, 10, Masanori Yamazaki 6, 10, Shinnya Uchino 7, 10, Shinichi Suzuki 8, 10, 小杉眞司 9, 10 Japanese Journal of Genetic Counseling 32(2): 93-93, 2011. |
From the results of questionary survey and the foreign countries investigation for discussion and proposal - researcher for improvement of the ethic guideline (Sansho guideline) about the P1-21 human genome, genetic analysis study - Ryuichi Ida 1, 高橋貴哲 2, Kazuto Kato 3 Japanese Journal of Genetic Counseling 32(2): 93-93, 2011. |
Genetic personal information that was found without intending in P1-22 human genome, a genetic analysis study, handling of the abnormality of the genes Tail moat Sachiko, History of plain tree, Mizuho Yamaguchi, Hamanoe spring, Hideaki Kato, Satoko Miyatake, Tano Island beauty castle, Mika Okuda, Kaori Sawai Japanese Journal of Genetic Counseling 32(2): 94-94, 2011. |
The present conditions of the Ethical Review Board about human genome, the genetic analysis study in the P1-23 medicine system university Way sum lily, 小杉眞司 Japanese Journal of Genetic Counseling 32(2): 94-94, 2011. |
Genetic counseling of the men who have been going to know the fact that P1-24 grass widow married again Kazuhiro Shiraishi, Kyoko Murashima Japanese Journal of Genetic Counseling 32(2): 94-94, 2011. |
Mainly on P1-25 registration of patient and the example of one discussion ... "tailor-made medicine realization project" about the role of the research coordinator in the follow-up 洪賢秀, Kaori Muto, 張瓊方, Maiko Watanabe Japanese Journal of Genetic Counseling 32(2): 95-95, 2011. |
The testing genetic for P1-26 public system application is ... from example experience of ... ball spinal cord stomach muscular dystrophy whether necessary 葛田衣重 1, 澤井摂 2, 3, 4, Emi Utsuno 2, 3, Kazumi Omachi 2, 3, Number of Kanai light 2, 3, 4, Satoshi Kuwahara 4, Akira Haneda 2, 3, Fumio Nomura 2, 3 Japanese Journal of Genetic Counseling 32(2): 95-95, 2011. |
Counselor authorization heredity - added to action - consultation person in charge team of the genetic counseling for hereditary neurologic intractable diseases in the P1-27 area Yasuko Yamauchi 1, Hideaki Chiyo 2, Jinichi Sawada 3, 4, Field original Kayo 4, 狭間敬憲 3, 4, Measure field Mitsuo 1, Yoshikazu Kuroki 1, Tatsushi Toda 5, 6 Japanese Journal of Genetic Counseling 32(2): 96-96, 2011. |
Analysis of the case in genetic counselling - Tokyo children nursing hospital of the P1-28 developmental disease Keiko Akaboshi, Toshihide Shiiki, Keiko Wada, Michiko Makino, Nobuyuki Takechi, Matsuda light exhibition, Michiko Takei, Saori Takeda, Hideji Matsui, Yasuko Nasu, Mitsuru Funahashi Toshiko, Yasuyuki Suzuki Japanese Journal of Genetic Counseling 32(2): 96-96, 2011. |
From the questionary survey to the parent of - adulthood patients looking back on childhood of the P1-29 Williams syndrome - Yuko Kito 1, 2, Shin Okazaki 3, Tomiwa Kiyotaka 1, 3, 4 Japanese Journal of Genetic Counseling 32(2): 97-97, 2011. |
Psychological effect - quantitative and qualitative study - that carrier diagnosis of the P1-30 structural chromosome aberration gives to the person and a family Minoru Kaneko Motoko 1, Hirofumi Ohashi 2, 篁倫子 1, 川目裕 1 Japanese Journal of Genetic Counseling 32(2): 97-97, 2011. |
An example of the Gitelman syndrome where new mutation was found by P1-31 genetic testing Tomoyoshi Nakayama 1, Naoyuki Sato 1, Joki Nobuhiko 2, Yasuko Yanagida 2, Tomori Tanaka 2, Description of Hiroshi Nagatani 2 Japanese Journal of Genetic Counseling 32(2): 97-97, 2011. |
P1-32 splice abnormal gene diagnosis - pit fall and approach method - Look at Nii; Hideki, Tomomi Ogawa, 野手良剛, Shiro Hayashi, Tomohiro Ueno, The Takeshi Harada right, Yoshinori Uji, Isao Kitajima Japanese Journal of Genetic Counseling 32(2): 98-98, 2011. |
Simultaneous analysis of two alcohol metabolism genetic polymorphism of P1-33 ADH1B, ALDH2 Yutaka Ota 1, Hirofumi Aruga 2, Sami study 1, Satoshi Kanda original 1, Junko Stevens2 Japanese Journal of Genetic Counseling 32(2): 98-98, 2011. |
Measurement and significance of the P1-34 disease-related genetic screening Ryuji Kawaguchi 1, Shizuka Kokubo 1, Makiko Watanabe 1, 澤谷桐子 1, 李昌珪 3, 櫻林郁之介 4 Japanese Journal of Genetic Counseling 32(2): 98-98, 2011. |
Genetic analysis of the odontogenic tumor that developed in P1-35 nevoid Basal cell carcinoma syndrome Toshiyuki Miyashita 1, Maiko Kiryu 1, Ryo Sasaki 2, Kayoko Saito 3, Katsunori Fujii 4 Japanese Journal of Genetic Counseling 32(2): 99-99, 2011. |
1 case of the hypotrichosis in acknowledgment of P1-36 LIPH mutation in the gene Sanae Numata 1, 2, 3, Takahiro Hamada 1, 2, 3, Harada なをみ 3, 4, 5, Tomoko Ohira 3, 4, Junko Watanabe 3, 4, Makoto Yoshino 3, 4, Yutaka Shimomura 6, Takashi Hashimoto 1, 2, 3 Japanese Journal of Genetic Counseling 32(2): 99-99, 2011. |
Experience the genetic counseling of the P1-37 xeroderma pigmentosum 2 case Emi Utsuno 1, Ayako Shimizu 2, Noriaki Kamata 2, Kobe direct intellect 2, Hiroyuki Matsue 2, Fumio Nomura 1 Japanese Journal of Genetic Counseling 32(2): 99-99, 2011. |
Genetic counseling of the incontinentia pigmenti families who assume P1-38 1-week-old neonates after birth proband Urakawa excellent work 1, Hermitage former Michiko 1, Yoshida eyes 1, Junko Tatsumi 1, 田村和朗 1, Kazuo Fujikawa 1, Shinichi Moriwaki 2 Japanese Journal of Genetic Counseling 32(2): 100-100, 2011. |
Analysis - of the content of information, the meeting question paper of support - parent that a parent, a family of the P1-39 "chromosome abnormal child" finds 勝元 Saeko 1, Arai A mind 2, Torishima Masako 2, 浦尾充子 1, Numabe Hironao 2, 小杉眞司 2 Japanese Journal of Genetic Counseling 32(2): 100-100, 2011. |
Genetic counseling of the example that had a sibling of the P1-40 Bardet-Biedl syndrome, and had a diagnosis of retinal pigment degeneration recently Kazumi Omachi 1, Akira Hagiwara 2, Akira Haneda 1, 3, Fumio Nomura 3 Japanese Journal of Genetic Counseling 32(2): 100-100, 2011. |
Fact-finding report about the homepage in the P2-01 whole country gene medical care section Komaki Masayasu 1, 2, Yuki Sato 1, Hamada Yusuke 1, 4, Takanobu Otomo 1, 4, Yoshizu Kikuko 1, 3, Country prefecture power 1, 6, Norio Sakai 1, 4, Noguchi Saburo Sana 1, 5 Japanese Journal of Genetic Counseling 32(2): 101-101, 2011. |
The present situation of the genetic counseling outpatient department in the P2-02 this hospital Yasuyuki Hasuo, Masanobu Ogawa Japanese Journal of Genetic Counseling 32(2): 101-101, 2011. |
Genetic counseling for P2-03 elderly people Yoko Okamoto 1, Yue Kanbara 1, Hiroko Mimura 1, Taku Kimura 2, Hiromi Nakata 1, 4, Tomoko Tamaoki 1, 3 Japanese Journal of Genetic Counseling 32(2): 101-101, 2011. |
About the present conditions of the genetic counseling in P2-04 a variety of culture 朱肖捷, 川目裕, 山本佳世乃 Japanese Journal of Genetic Counseling 32(2): 102-102, 2011. |
Cooperation of a psychology job and the nursing profession in the P2-05 heredity outpatient department Mariko Tamai, Hiromi Yamashita, Asako Mizuuchi, Yoshimitsu Fukushima Japanese Journal of Genetic Counseling 32(2): 102-102, 2011. |
Effect of the life story interview to a client concerned with P2-06 inherited disease 山本佳世乃, 川目裕 Japanese Journal of Genetic Counseling 32(2): 102-102, 2011. |
Pay the attention to affector - to counselee in the P2-07 genetic counseling particularly a non-language; and - Junko Tatsumi 1, 2, Carrying box Yuri 2 Japanese Journal of Genetic Counseling 32(2): 103-103, 2011. |
About lack of understanding and misunderstanding for the genetic information of counselee and the family with the P2-08 inherited disease Satoshi Fukano sinter, 山本佳世乃, 川目裕 Japanese Journal of Genetic Counseling 32(2): 103-103, 2011. |
The way of the genetic screening studies education in the P2-09 medical technologist training course Hideshi Kanzaki Japanese Journal of Genetic Counseling 32(2): 103-103, 2011. |
Discussion that we maintain understanding - tutorial for the prenatal diagnosis of the P2-10 medical student Kondo vermilion sound 1, 2, Yuko Onuki 2, Shigeru Sato 1, 2, Takahashi Senka 1, 2, Yumiko Goto 1, 2, Mitsuko Mizoguchi 2, Shunichiro Izumi 1, 2 Japanese Journal of Genetic Counseling 32(2): 104-104, 2011. |
Is the VCR seeing and hearing that we described P2-11 Down's syndrome in useful in genetic counseling about the prenatal diagnosis? Naoya Hashimoto 1, Kumagami Atsuko 2, Yoko Horiuchi 2, Kyoko Shiota 2, Isao Kusakawa 3, Yoshiko Kusama 2, Mikiko Yoshino 2, Arimori Naoko 2, Michiko Yamanaka 2, Kodo Sato 2, Yasushi Ishida 3 Japanese Journal of Genetic Counseling 32(2): 104-104, 2011. |
Questionnaire about the diagnosis notice of P2-12 Down's syndrome Kiyoko Samejima 1, Yasuhide Hayashi 2 Japanese Journal of Genetic Counseling 32(2): 104-104, 2011. |
Investigation about the adult health care with P2-13 Down's syndrome Kimiko Ueda 1, Nobuhiko Okamoto 2, Tetsu Hirayama 3, Junko Tatsumi 4, Keiko Matsuda 2, Akimaru Noriko 2, Yuko Mishima 2, Atsuko Ikegawa 2, Shiro Sagawa 5 Japanese Journal of Genetic Counseling 32(2): 105-105, 2011. |
Activity of the P2-14 Nagano Prefectural children Hospital Down's syndrome group outpatient department Keiko Arakawa Japanese Journal of Genetic Counseling 32(2): 105-105, 2011. |
Monovular twins case of mosaicism trisomy 21 that Down's syndrome, other one child presented with a normal phenotype P2-15 one child Junko Mochizuki 1, 4, Kitsunezaki Masako 2, 4, Kan Amano 1, Shinya Umino 1, History of Takada man 3, 4 Japanese Journal of Genetic Counseling 32(2): 105-105, 2011. |
Decision-making dilemma for the surgical cure of congenital heart disease complicated with P2-16 Down's syndrome Kenji Shimizu 1, Misako Kojima 1, Hirofumi Ohashi 1, Kiyoshi Ogawa 2, Chiaki Kakinuma 3, Akemi Hirano 3 Japanese Journal of Genetic Counseling 32(2): 106-106, 2011. |
Gene diagnosis of P2-17 tardive neurofibromatosis (NF7) Shinki Uchiyama, Sakai Noriyasu, Tatsuro Maeda, Ryoji Tsuboi, Yoshihiko Mitsuhashi Japanese Journal of Genetic Counseling 32(2): 106-106, 2011. |
The reproductive medicine for women with P2-18 Turner's syndrome and the problems Takeshi Hashiba, Kaori Takahashi, Taku Sato, Hiroshi Sueoka, Yasusuke Yoshimura Japanese Journal of Genetic Counseling 32(2): 106-106, 2011. |
One case of the 4p - syndrome that presented with the fetal growth failure in the P2-19 altitude uterus, and led to intra-uterine death Mizuho Yamaguchi 1, Mika Okuda 1, Akihiko Mochizuki 1, Tano Island beauty castle 1, Kurasawa Kentaro 1, Tsuneo Takahashi 1, History of plain tree 2, Husband Ritsuko 3 Japanese Journal of Genetic Counseling 32(2): 107-107, 2011. |
Discussion about the 3 case that we cooperated, and 18Trisomy was diagnosed by of heredity diagnosis and treatment department and the maternity ward nurse midwife in the P2-20 this hospital Yumiko Goto 1, 2, Kondo vermilion sound 1, 2, Yuko Onuki 2, Hiromi Moriya 2, Keiko Tsuji 2, Hiroko Yokoyama 2, Mitsuko Mizoguchi 2, Shunichiro Izumi 1, 2 Japanese Journal of Genetic Counseling 32(2): 107-107, 2011. |
8p23.2 and discussion about the 9q13-q21 duplication that we detected by P2-21 examination using ammiotic fluid Yuki Sasaki 1, 霜川修 1, Takeshi Matsui 1, Old volost Yuka child 2, 上塘正人 2, Naoki Harada 1 Japanese Journal of Genetic Counseling 32(2): 107-107, 2011. |
Genetic counseling of P2-22 dic (12, 22) Numabe Hironao 1, 2, 勝元 Saeko 1, Takahiro Nakayama 3 Japanese Journal of Genetic Counseling 32(2): 108-108, 2011. |
The support that delivery and the gene practice moiety of children with P2-23 anencephalia are available for Hiromi Yamashita, Mariko Tamai, Tomoki Kosho, Yoshimitsu Fukushima Japanese Journal of Genetic Counseling 32(2): 108-108, 2011. |
Ratio of neonates with congenital anomalies admitted to the P2-24 Osaka City comprehensive medical care center NICU Midori Fujita Japanese Journal of Genetic Counseling 32(2): 108-108, 2011. |
Hereditary multiple exostosis by the P2-25 8q24 deletion and 1, boys case who had 19 translocation type preceding B cells-related lymphocytic leukemia 中根貴弥 1, 2, 合井久美子 2, Kanji Sugita 1, 2 Japanese Journal of Genetic Counseling 32(2): 109-109, 2011. |
It is a present conditions report and the examination about the disease name P2-26 lethality osteodysplasty 岡要 1, Hideaki Sawai 2, Numabe Hironao 3, 浦尾充子 1, 小杉眞司 1, Masahiko Kawai 4 Japanese Journal of Genetic Counseling 32(2): 109-109, 2011. |
Genetic counseling for the P2-27 achondrogenesis merger pregnant woman Osamu Samura 1, Tomoya Mizunoe 1, Satoshi Okamoto 1, 數佐淑恵 1, Hiroko Nakamura 1, Yosuke Kawakami 1, Kazuhiro Takehara 1, Maki Hyodo 2 Japanese Journal of Genetic Counseling 32(2): 109-109, 2011. |
1 case of the ornithine transcarbamylase deficiency carrier pregnant woman who racked the brains about P2-28 counseling Tomoko Taniguchi 1, Naoki Takeshita 2, Yukiko Katagiri 1, Chizu Aoki 1, Azusa Moriyama 1, Masanobu Tanaka 1, Alien from Morita peak 1 Japanese Journal of Genetic Counseling 32(2): 110-110, 2011. |
Literature examination about the psychosocial problem in adult patients with P2-29 Fabry's disease Yuri Yasuda, 山本佳世乃, 川目裕 Japanese Journal of Genetic Counseling 32(2): 110-110, 2011. |
Genetic counseling with the neonatal mass screening enforcement of P2-30 lysosome disease Akemi Tanaka 1, Takeshi Suzuki 2, Torayuki Okuyama 3, Satoshi Sawada 1, Tomoko Sakaguchi 1, Eri Oda 3, Ken Fujikawa person 2, wisteria Naoko 3, Mika Saito 1, Teruo Kitagawa 2 Japanese Journal of Genetic Counseling 32(2): 110-110, 2011. |
The present conditions and problems of the amniotic fluid chromosome banding in the P2-31 Miyagi Prefectural children Hospital 宮下進 1, Katsunori Ozawa 1, 2, Satoshi Sato Jiro 1, 2, 室月淳 1, 2 Japanese Journal of Genetic Counseling 32(2): 111-111, 2011. |
Heredity counseling office visiting rate by "the pregnancy with advanced maternal age" in P2-32 high level and the community medical care organization, comparison of the amniotic diagnosis rate of use 中村博昭1, 3, 本久智賀2, 3, 渡邉通子3, 依藤亨3, 富和清隆3 Japanese Journal of Genetic Counseling 32(2): 111-111, 2011. |
We examine illness in the prenatal diagnosis of the P2-33 this hospital and cooperate Takahashi Senka 1, 2, Kondo vermilion sound 1, 2, Shigeru Sato 1, 2, Yumiko Goto 1, 2, Hiromi Moriya 1, Hiroko Yokoyama 1, Shunichiro Izumi 1, 2 Japanese Journal of Genetic Counseling 32(2): 112-112, 2011. |
Summary - in our prenatal diagnosis - center of the P2-34 structural chromosome aberration carrier of 10 years Michiko Watanabe 1, 本久智賀 1, 2, Hiroaki Nakamura 1, 3, Tomiwa Kiyotaka 1, 4 Japanese Journal of Genetic Counseling 32(2): 112-112, 2011. |
Pit fall case in the amniotic fluid chromosome banding that P2-35 many institutions are involved in Hisao Nagata 1, 2, Sachi Yamaji 1, Akiko Omoto 1, Emi Utsuno 2, 3, Fumio Nomura 2, 3, 4 Japanese Journal of Genetic Counseling 32(2): 113-113, 2011. |
The present conditions of the genetic counselling outpatient department in the P2-36 low risk pregnancy handling institution over Nuchal Traslucency (following NT) screening: Capital former Akiko, Akira Yamaguchi Japanese Journal of Genetic Counseling 32(2): 113-113, 2011. |
Prenatal diagnosis experience of the autosomalrecessive polycystic kidney disease that caused the recurrence in the P2-37 sibling The Kotobuki, Ikuno history, Itsukaichi Mina, Izumi Oki, Takeshi Serikawa University, Koichi Takakuwa, Kenichi Tanaka Japanese Journal of Genetic Counseling 32(2): 113-113, 2011. |
Micrencephaly with P2-38 pontcerebellum hypoplasia, mutation analysis of the CASK gene in the mental retadation Yuto Yamamoto 1, 林深 2, Rice Joji Sawa 2, Hiroaki Ono 3, Shuichi Shimakawa 4, Yukitoshi Takahashi 5, Seiji Mizuno 6, Nobuhiko Okamoto 1 Japanese Journal of Genetic Counseling 32(2): 114-114, 2011. |
Ventricular morphometrical analysis in the P2-39 human embryo stage Tetsuya Takakuwa 1, Takashi Nakajima 1, Naoki Shiraishi 1, Shigeto Yamada 2, Upper part Chikako 2, Kohei Shiota 2, Katsumi Kose 3 Japanese Journal of Genetic Counseling 32(2): 114-114, 2011. |
Genetic counseling for the precritical new age when it was diagnosed and fixed our eyes on the spread and therapeutic drug development of the gene diagnosis of Duchenne dystrophy at P2-40 1 year old Takeo Kubota 1, 中根貴弥 1, Mariko Nakamura 1, Mariko Tamai 1, 石黒浩毅 1, Satoko Nakagome 1, Kanji Sugita 1, Hirofumi Komaki 2 Japanese Journal of Genetic Counseling 32(2): 114-114, 2011. |