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- [1] Secondary And Incidental Findings in A Cohort of Patients with Immune-Mediated Disease Undergoing Exome SequencingJOURNAL OF CLINICAL IMMUNOLOGY, 2020, 40 (SUPPL 1) : S38 - S39Setzer, Michael论文数: 0 引用数: 0 h-index: 0机构: NIAID, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA Med Sci & Comp LLC, Bethesda, MD USA NIAID, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USASimiluk, Morgan论文数: 0 引用数: 0 h-index: 0机构: NIAID, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA NIAID, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USAWalkiewicz, Magdalena论文数: 0 引用数: 0 h-index: 0机构: NIAID, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA NIAID, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USAHolland, Steven论文数: 0 引用数: 0 h-index: 0机构: NIAID, Div Intramural Res, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA NIAID, Immunopathogenesis Sect, Lab Clin Immunol & Microbiol LCIM, Div Intramural Res DIR,NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA NIAID, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
- [2] Secondary findings of exome sequencing in Russian patientsEUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 568 - 569Mironovich, Olga论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaGundorova, Polina论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaCherevatova, Tatyana论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaOrlova, Anna论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaZabnenkova, Viktoria论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaChuhrova, Alena论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaPoliakov, Aleksander论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaRyzhkova, Oxana论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, Russia
- [3] Exploring the Impact of Genetics in a Large Cohort of Moebius Patients by Trio Whole Exome SequencingGENES, 2024, 15 (08)Moresco, Giada论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyBedeschi, Maria Francesca论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Med Genet Unit, I-20122 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyVenturin, Marco论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Med Biotechnol & Translat Med, I-20054 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyVilla, Roberta论文数: 0 引用数: 0 h-index: 0机构: ASST Santi Paolo & Carlo, Med Genet Unit, I-20142 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyCostanza, Jole论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Res Labs Coordinat Unit, I-20122 Milan, Italy Nerviano Med Sci, Biol Dept, Viale Pasteur 10, I-20014 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyMauri, Alessia论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Res Labs Coordinat Unit, I-20122 Milan, Italy Univ Milan, Pediat Clin Res Ctr Romeo & Enrica Invernizzi, Dept Biomed & Clin Sci, I-20157 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalySantaniello, Carlo论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Res Labs Coordinat Unit, I-20122 Milan, Italy Ctr Diagnost Italiano, Lab Med Genet, I-20147 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyPicciolini, Odoardo论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Pediat Phys Med & Rehabil Unit, I-20122 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyMessina, Laura论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Pediat Phys Med & Rehabil Unit, I-20122 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyTriulzi, Fabio论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neuroradiol Unit, I-20122 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyMiozzo, Monica Rosa论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, Italy ASST Santi Paolo & Carlo, Med Genet Unit, I-20142 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyRondinone, Ornella论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, ItalyFontana, Laura论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, Italy ASST Santi Paolo & Carlo, Med Genet Unit, I-20142 Milan, Italy Univ Milan, Dept Hlth Sci, Med Genet, I-20142 Milan, Italy
- [4] Whole exome sequencing in a cohort of adults patients with intellectual disabilityEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1391 - 1391Marey, I.论文数: 0 引用数: 0 h-index: 0机构: Med Genet UF, AP HP, Genet Dept, Paris, France Reference Ctr Intellectual Disabil Rare Causes, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceHeide, S.论文数: 0 引用数: 0 h-index: 0机构: Med Genet UF, AP HP, Genet Dept, Paris, France Reference Ctr Intellectual Disabil Rare Causes, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceMignot, C.论文数: 0 引用数: 0 h-index: 0机构: Med Genet UF, AP HP, Genet Dept, Paris, France Reference Ctr Intellectual Disabil Rare Causes, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceWhalen, S.论文数: 0 引用数: 0 h-index: 0机构: Med Genet UF, AP HP, Genet Dept, Paris, France Reference Ctr Intellectual Disabil Rare Causes, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceAfenjar, A.论文数: 0 引用数: 0 h-index: 0机构: Med Genet UF, AP HP, Genet Dept, Paris, France Reference Ctr Intellectual Disabil Rare Causes, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceBuratti, J.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dev Genom UF, Genet Dept, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceOlin, V.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dev Genom UF, Genet Dept, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceLejeune, E.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dev Genom UF, Genet Dept, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceKaragic, S.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dev Genom UF, Genet Dept, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceNava, C.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dev Genom UF, Genet Dept, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceSpentchian, M.论文数: 0 引用数: 0 h-index: 0机构: Reference Ctr Intellectual Disabil Rare Causes, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceHeron, D.论文数: 0 引用数: 0 h-index: 0机构: Med Genet UF, AP HP, Genet Dept, Paris, France Reference Ctr Intellectual Disabil Rare Causes, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceKeren, B.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dev Genom UF, Genet Dept, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, FranceCharles, P.论文数: 0 引用数: 0 h-index: 0机构: Med Genet UF, AP HP, Genet Dept, Paris, France Reference Ctr Intellectual Disabil Rare Causes, Paris, France Med Genet UF, AP HP, Genet Dept, Paris, France
- [5] Review of secondary findings reported in the qGenomics patient cohort, analyzed by exome sequencingEUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 574 - 574Carreno, Marta论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainSegura-Puimedon, Maria论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainGarcia, Raquel论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainCarreno, Lidia论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainArjona, Cesar论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainNicolas, Hector San论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainSintas, Celia论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainVall, Monica论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainMarcos, Olaya Villa论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainVinas-Jornet, Marina论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainArmengol, Lluis论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, Spain
- [6] Molecular findings in patients for whole exome sequencing and mitochondrial genome assessmentCLINICA CHIMICA ACTA, 2024, 561Sun, Gege论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R China Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R ChinaHuang, Wei论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R China Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R ChinaWang, Li论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R China Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R ChinaWu, Jinlin论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R China Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R ChinaZhao, Ganye论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R China Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R ChinaRen, Huanan论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R China Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R ChinaLiu, Lina论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R China Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R ChinaKong, Xiangdong论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R China Zhengzhou Univ, Genet & Prenatal Diag Ctr, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R China
- [7] Whole Exome Sequencing in a Cohort of Unsolved LeukodystrophiesANNALS OF NEUROLOGY, 2014, 76 : S193 - S193Helman, G.论文数: 0 引用数: 0 h-index: 0Simons, C.论文数: 0 引用数: 0 h-index: 0Pizzino, A.论文数: 0 引用数: 0 h-index: 0Murphy, J.论文数: 0 引用数: 0 h-index: 0Bloom, M.论文数: 0 引用数: 0 h-index: 0Evans, S.论文数: 0 引用数: 0 h-index: 0Taft, R.论文数: 0 引用数: 0 h-index: 0Vanderver, A.论文数: 0 引用数: 0 h-index: 0
- [8] Incidental and secondary findings in trio exome sequencingGENES & DISEASES, 2024, 11 (04)Cohen, Camille论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, FranceBellanger, Emeline论文数: 0 引用数: 0 h-index: 0机构: RHuMA, UMR BREED, INRA ENVA UVSQ, F-78180 Montigny le Bretonneux, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, FranceMortreux, Jeremie论文数: 0 引用数: 0 h-index: 0机构: Lab Eurofins Biomnis, Serv Genet, F-69007 Lyon, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, FranceRaymond, Laure论文数: 0 引用数: 0 h-index: 0机构: Lab Eurofins Biomnis, Serv Genet, F-69007 Lyon, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, FranceVialard, Francois论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, France RHuMA, UMR BREED, INRA ENVA UVSQ, F-78180 Montigny le Bretonneux, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, FranceDard, Rodolphe论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, France
- [9] Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patientsHUMAN GENETICS, 2021, 140 (02) : 321 - 331Horiuchi, Yasue论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, Japan Tokyo Metropolitan Inst Med Sci, Dept Psychiat & Behav Sci, Tokyo, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanMatsubayashi, Hiroyuki论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanKiyozumi, Yoshimi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanNishimura, Seiichiro论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanHigashigawa, Satomi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanKado, Nobuhiro论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanNagashima, Takeshi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr, Res Inst, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanMizuguchi, Maki论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr, Res Inst, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanOhnami, Sumiko论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr, Res Inst, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanArai, Makoto论文数: 0 引用数: 0 h-index: 0机构: Tokyo Metropolitan Inst Med Sci, Dept Psychiat & Behav Sci, Tokyo, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanUrakami, Kenichi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr, Res Inst, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanKusuhara, Masatoshi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr, Res Inst, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, JapanYamaguchi, Ken论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Canc Ctr, Res Inst, Shizuoka, Japan Shizuoka Canc Ctr Hosp, Div Genet Counseling, Genet Med Promot, Shizuoka, Japan
- [10] Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patientsHuman Genetics, 2021, 140 : 321 - 331Yasue Horiuchi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionHiroyuki Matsubayashi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionYoshimi Kiyozumi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionSeiichiro Nishimura论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionSatomi Higashigawa论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionNobuhiro Kado论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionTakeshi Nagashima论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionMaki Mizuguchi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionSumiko Ohnami论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionMakoto Arai论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionKenichi Urakami论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionMasatoshi Kusuhara论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine PromotionKen Yamaguchi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Cancer Center Hospital,Division of Genetic Counseling, Genetic Medicine Promotion