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- [1] Tumor Spectrum in Children With Noonan Syndrome and SOS1 or RAF1 Mutations[J]. GENES CHROMOSOMES & CANCER, 2010, 49 (03): : 242 - 252Denayer, Ellen论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Louvain, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumDevriendt, Koen论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Louvain, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, Belgiumde Ravel, Thomy论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Louvain, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumVan Buggenhout, Griet论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Louvain, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumSmeets, Eric论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Louvain, Belgium Univ Limburg, Acad Hosp Maastricht, Dept Clin Genet, Maastricht, Netherlands Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumFrancois, Inge论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven Hosp, Dept Pediat, Louvain, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumSznajer, Yves论文数: 0 引用数: 0 h-index: 0机构: ULB, Hop Univ Enfants Reine Fabiola HUDERF, Pediat Clin Genet & Ctr Human Genet, Brussels, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumCraen, Margarita论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Dept Pediat Endocrinol, B-9000 Ghent, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumLeventopoulos, George论文数: 0 引用数: 0 h-index: 0机构: Univ Athens, Sch Med, Aghia Sophia Childrens Hosp, Dept Med Genet, GR-11527 Athens, Greece Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumMutesa, Leon论文数: 0 引用数: 0 h-index: 0机构: Univ Liege, CHU Sart Tilman, Univ Hosp Ctr, Ctr Human Genet, Liege, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumVandecasseye, Willy论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven Hosp, Dept Pediat, Louvain, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumMassa, Guy论文数: 0 引用数: 0 h-index: 0机构: Virga Jesseziekenhuis, Dept Pediat, Hasselt, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumKayserili, Hulya论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Istanbul Fac Med, Dept Med Genet, Istanbul, Turkey Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumSciot, Raf论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Pathol, Louvain, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumFryns, Jean-Pierre论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Louvain, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, BelgiumLegius, Eric论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Louvain, Belgium Katholieke Univ Leuven, Dept Human Genet, Louvain, Belgium
- [2] Noonan Syndrome Associated With Both a New Jnk-Activating Familial SOS1 and a De Novo RAF1 Mutations[J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (09) : 2176 - 2184Longoni, Mauro论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyMoncini, Silvia论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyCisternino, Mariangela论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Policlin San Matteo, Dipartimento Pediat, Fdn IRCCS, I-27100 Pavia, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyMorella, Ilaria M.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, MI, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyFerraiuolo, Serena论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Auxol Italiano, Milan, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyRusso, Silvia论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Auxol Italiano, Milan, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyMannarino, Savina论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Policlin San Matteo, Dipartimento Pediat, Fdn IRCCS, I-27100 Pavia, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyBrazzelli, Valeria论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Policlin San Matteo, Dipartimento Patol Umana Ereditaria, Ist Dermatol,Fdn IRCCS, I-27100 Pavia, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyCoi, Paola论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Policlin San Matteo, Dipartimento Pediat, Fdn IRCCS, I-27100 Pavia, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyZippel, Renata论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, MI, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyVenturin, Marco论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, ItalyRiva, Paola论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, Italy Univ Milan, Dept Biol & Genet Med Sci, I-20133 Milan, MI, Italy
- [3] Mutation analysis in a group of patients with Noonan syndrome, new mutations identified in SOS1[J]. HORMONE RESEARCH, 2008, 70 : 42 - 42Cisternino, Mariangela论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, Italy Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, ItalyLongoni, Mauro论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, Italy Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, ItalyCoi, Paola论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, Italy Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, ItalyMannarino, Savina论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Policlin S Matteo, Unit Pediat Cardiol, Pavia, Italy Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, ItalyCabano, Rita论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, Italy Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, ItalySirgiovanni, Ida论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, Italy Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, ItalyRulfi, Gabriele论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, Italy Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, ItalyRiva, Paola论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Biol & Genet, Milan, Italy Univ Pavia, Dept Pediat, Fdn IRCCS Pol S Matteo, I-27100 Pavia, Italy
- [4] Mutations in the RAF1 gene are associated with hypertrophic cardiomyopathy in Noonan syndrome[J]. JOURNAL OF MEDICAL GENETICS, 2007, 44 : S25 - S25Razzaque, Abdur论文数: 0 引用数: 0 h-index: 0机构: Waseda Univ, Sch Med, Dept Biol, Tokyo, Japan Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, JapanNishizawa, T.论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, Japan Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, JapanKomoike, Y.论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, Japan Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, JapanYagi, H.论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, Japan Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, JapanFurutani, M.论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, Japan Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, JapanAmo, R.论文数: 0 引用数: 0 h-index: 0机构: Waseda Univ, Sch Med, Dept Biol, Tokyo, Japan Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, JapanHigashinakagawa, T.论文数: 0 引用数: 0 h-index: 0机构: Waseda Univ, Sch Med, Dept Biol, Tokyo, Japan Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, JapanMatsuoka, R.论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, Japan Tokyo Womens Med Univ, Int Res & Educ Inst Integrat Med Sci IREIIMS, Tokyo, Japan
- [5] Noonan syndrome with RAF1 gene mutations in a newborn with cerebral haemorrhage[J]. European Journal of Medical Research, 27Junwei Lan论文数: 0 引用数: 0 h-index: 0机构: Research Group in Lishui Municipal Central Hospital of Zhejiang Province,Neonatology DepartmentTianbao Zeng论文数: 0 引用数: 0 h-index: 0机构: Research Group in Lishui Municipal Central Hospital of Zhejiang Province,Neonatology DepartmentSheng Liu论文数: 0 引用数: 0 h-index: 0机构: Research Group in Lishui Municipal Central Hospital of Zhejiang Province,Neonatology DepartmentJuhong Lan论文数: 0 引用数: 0 h-index: 0机构: Research Group in Lishui Municipal Central Hospital of Zhejiang Province,Neonatology DepartmentLijun Qian论文数: 0 引用数: 0 h-index: 0机构: Research Group in Lishui Municipal Central Hospital of Zhejiang Province,Neonatology Department
- [6] Noonan syndrome with RAF1 gene mutations in a newborn with cerebral haemorrhage[J]. EUROPEAN JOURNAL OF MEDICAL RESEARCH, 2022, 27 (01)Lan, Junwei论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Res Grp, Lishui Municipal Cent Hosp Zhejiang Prov, Neonatol Dept,Lishui Hosp, Lishui 323000, Peoples R China Zhejiang Univ, Res Grp, Lishui Municipal Cent Hosp Zhejiang Prov, Neonatol Dept,Lishui Hosp, Lishui 323000, Peoples R ChinaZeng, Tianbao论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Res Grp, Lishui Municipal Cent Hosp Zhejiang Prov, Neonatol Dept,Lishui Hosp, Lishui 323000, Peoples R China Zhejiang Univ, Res Grp, Lishui Municipal Cent Hosp Zhejiang Prov, Neonatol Dept,Lishui Hosp, Lishui 323000, Peoples R ChinaLiu, Sheng论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Res Grp, Lishui Municipal Cent Hosp Zhejiang Prov, Neonatol Dept,Lishui Hosp, Lishui 323000, Peoples R China Zhejiang Univ, Res Grp, Lishui Municipal Cent Hosp Zhejiang Prov, Neonatol Dept,Lishui Hosp, Lishui 323000, Peoples R ChinaLan, Juhong论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Res Grp, Lishui Municipal Cent Hosp Zhejiang Prov, Neonatol Dept,Lishui Hosp, Lishui 323000, Peoples R China Zhejiang Univ, Res Grp, Lishui Municipal Cent Hosp Zhejiang Prov, Neonatol Dept,Lishui Hosp, Lishui 323000, Peoples R ChinaQian, Lijun论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Res Grp, Lishui Municipal Cent Hosp Zhejiang Prov, Neonatol Dept,Lishui Hosp, Lishui 323000, Peoples R China Zhejiang Univ, Res Grp, Lishui Municipal Cent Hosp Zhejiang Prov, Neonatol Dept,Lishui Hosp, Lishui 323000, Peoples R China
- [7] RAF-1 Mutation Associated with a Risk for Ventricular Arrhythmias in a Child with Noonan Syndrome and Cardiovascular Pathology[J]. JOURNAL OF CRITICAL CARE MEDICINE, 2022, 8 (02): : 126 - 130Fagarasan, Amalia论文数: 0 引用数: 0 h-index: 0机构: George Emil Palade Univ Med Pharm Sci & Technol T, Targu Mures, Romania George Emil Palade Univ Med Pharm Sci & Technol T, Targu Mures, RomaniaAl Hussein, Hamida论文数: 0 引用数: 0 h-index: 0机构: George Emil Palade Univ Med Pharm Sci & Technol T, Targu Mures, Romania George Emil Palade Univ Med Pharm Sci & Technol T, Targu Mures, RomaniaGhiragosian Rusu, Simina Elena论文数: 0 引用数: 0 h-index: 0机构: George Emil Palade Univ Med Pharm Sci & Technol T, Targu Mures, Romania George Emil Palade Univ Med Pharm Sci & Technol T, Targu Mures, Romania
- [8] Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome[J]. JOURNAL OF HUMAN GENETICS, 2008, 53 (09) : 834 - 841Narumi, Yoko论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanAoki, Yoko论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanNiihori, Tetsuya论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanSakurai, Masahiro论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Grad Sch Med, Dept Cardiovasc Surg, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanCave, Helene论文数: 0 引用数: 0 h-index: 0机构: Hop Robert Debre, APHP, Dept Genet, F-75019 Paris, France Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanVerloes, Alain论文数: 0 引用数: 0 h-index: 0机构: Hop Robert Debre, APHP, Dept Genet, F-75019 Paris, France Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanNishio, Kimio论文数: 0 引用数: 0 h-index: 0机构: Seirei Hamamatsu Gen Hosp, Dept Clin Genet, Hamamatsu, Shizuoka, Japan Nishio Family Clin, Hamamatsu, Shizuoka, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanOhashi, Hirofumi论文数: 0 引用数: 0 h-index: 0机构: Saitama Childrens Med Ctr, Div Med Genet, Saitama, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanKurosawa, Kenji论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanOkamoto, Nobuhiko论文数: 0 引用数: 0 h-index: 0机构: Osaka Med Ctr, Dept Planning & Res, Osaka, Japan Res Inst Maternal & Child Hlth, Osaka, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanKawame, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Nagano Childrens Hosp, Div Med Genet, Nagano, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanMizuno, Seiji论文数: 0 引用数: 0 h-index: 0机构: Cent Hosp, Dept Pediat, Aichi Human Serv Ctr, Aichi, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanKondoh, Tatsuro论文数: 0 引用数: 0 h-index: 0机构: Misakaenosono Mutsumi Dev Med & Welf Ctr, Div Dev Disabil, Isahaya, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanAddor, Marie-Claude论文数: 0 引用数: 0 h-index: 0机构: CHU Vaudois, Dept Med Genet, Lausanna, Switzerland Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanCoeslier-Dieux, Anne论文数: 0 引用数: 0 h-index: 0机构: CHRU, Dept Med Genet, Lille, France Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanVincent-Delorme, Catherine论文数: 0 引用数: 0 h-index: 0机构: CH Arras, Arras, France Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanTabayashi, Koichi论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Grad Sch Med, Dept Cardiovasc Surg, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanAoki, Masashi论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Neurol, Grad Sch Med, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanKobayashi, Tomoko论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanGuliyeva, Afag论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanKure, Shigeo论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, JapanMatsubara, Yoichi论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, Japan
- [9] Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome[J]. Journal of Human Genetics, 2008, 53 : 834 - 841Yoko Narumi论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsYoko Aoki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsTetsuya Niihori论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsMasahiro Sakurai论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsHélène Cavé论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsAlain Verloes论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsKimio Nishio论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsHirofumi Ohashi论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsKenji Kurosawa论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsNobuhiko Okamoto论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsHiroshi Kawame论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsSeiji Mizuno论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsTatsuro Kondoh论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsMarie-Claude Addor论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsAnne Coeslier-Dieux论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsCatherine Vincent-Delorme论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsKoichi Tabayashi论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsMasashi Aoki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsTomoko Kobayashi论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsAfag Guliyeva论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsShigeo Kure论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsYoichi Matsubara论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical Genetics
- [10] Germline gain-of-function mutations in SOS1 cause Noonan syndrome[J]. Nature Genetics, 2007, 39 : 70 - 74Amy E Roberts论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of MedicineToshiyuki Araki论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of MedicineKenneth D Swanson论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of MedicineKate T Montgomery论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of MedicineTaryn A Schiripo论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of MedicineVictoria A Joshi论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of MedicineLi Li论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of MedicineYosuf Yassin论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of MedicineAlex M Tamburino论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of MedicineBenjamin G Neel论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of MedicineRaju S Kucherlapati论文数: 0 引用数: 0 h-index: 0机构: Harvard Partners Center for Genetics and Genomics and Harvard Medical School,Division of Genetics, Department of Medicine