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- [1] Cognitive profile of a child with SOS1 mutation in Noonan syndromeNEUROLOGIA, 2018, 33 (02): : 137 - 138Martinez Planello, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Madrid, Dept Psicol Basica, Madrid, Spain Univ Autonoma Madrid, Dept Psicol Basica, Madrid, SpainSotillo, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Madrid, Dept Psicol Basica, Madrid, Spain Univ Autonoma Madrid, Dept Psicol Basica, Madrid, SpainRodriguez-Santos, F.论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Madrid, Dept Psicol Basica, Madrid, Spain Equipo Especif Discapacidad Motora, Consejeria Educ, Madrid, Spain Univ Autonoma Madrid, Dept Psicol Basica, Madrid, Spain
- [2] Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndromeJOURNAL 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, Japan论文数: 引用数: h-index:机构:Sakurai, 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, Japan论文数: 引用数: h-index:机构:Kobayashi, 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
- [3] Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndromeJournal 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
- [4] EMBRYONAL RHABDOMYOSARCOMA IN A PATIENT WITH NOONAN SYNDROME AND A SOS1 GERMLINE MUTATIONCELLULAR ONCOLOGY, 2010, 32 (03) : 195 - 195Jongmans, M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsHoogerbrugge, P.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsHilkens, L.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsFlucke, U.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlandsvan der Burgt, I.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsNoordam, K.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsRuiterkam-Versteeg, M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsYntema, H.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsNillesen, W.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsLigtenberg, M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsGeurts-van Kessel, A.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsKuiper, R.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, NetherlandsHoogerbrugge, N.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands
- [5] A Further Patient with Noonan Syndrome Due to a SOS1 Mutation and RhabdomyosarcomaGENES CHROMOSOMES & CANCER, 2010, 49 (10): : 967 - 968Hastings, Rob论文数: 0 引用数: 0 h-index: 0机构: Bristol Royal Hosp Children, Dept Clin Genet, Bristol, Avon, England Bristol Royal Hosp Children, Dept Clin Genet, Bristol, Avon, EnglandNewbury-Ecob, Ruth论文数: 0 引用数: 0 h-index: 0机构: Bristol Royal Hosp Children, Dept Clin Genet, Bristol, Avon, England Bristol Royal Hosp Children, Dept Clin Genet, Bristol, Avon, EnglandNg, Antony论文数: 0 引用数: 0 h-index: 0机构: Bristol Royal Hosp Children, Dept Pediat Oncol, Bristol, Avon, England Bristol Royal Hosp Children, Dept Clin Genet, Bristol, Avon, EnglandTaylor, Rohan论文数: 0 引用数: 0 h-index: 0机构: St George Hosp, SW Thames Mol Genet Lab, London, England Bristol Royal Hosp Children, Dept Clin Genet, Bristol, Avon, England
- [6] A case of Noonan Syndrome with coeliac disease due to SOS1 mutationMEDICINA CLINICA, 2011, 137 (14): : 666 - 667Carcavilla Urqui, Atilano论文数: 0 引用数: 0 h-index: 0机构: Hosp Virgen de la Salud, Serv Pediat, Toledo, Spain Hosp Gen Univ Gregorio Maranon, Serv Bioquim, Genet Mol Lab, Madrid, Spain Hosp Virgen de la Salud, Serv Pediat, Toledo, SpainSantome Collazo, Jose Luis论文数: 0 引用数: 0 h-index: 0机构: Hosp Gen Univ Gregorio Maranon, Serv Bioquim, Genet Mol Lab, Madrid, Spain Hosp Virgen de la Salud, Serv Pediat, Toledo, SpainBarrio Castellanos, Raquel论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Ramon y Cajal, Madrid, Spain Hosp Virgen de la Salud, Serv Pediat, Toledo, SpainEzquieta Zubicaray, Begona论文数: 0 引用数: 0 h-index: 0机构: Hosp Gen Univ Gregorio Maranon, Serv Bioquim, Genet Mol Lab, Madrid, Spain Inst Salud Carlos III, CIBERER, Madrid, Spain Hosp Virgen de la Salud, Serv Pediat, Toledo, Spain
- [7] Germline gain-of-function mutations in SOS1 cause Noonan syndromeNature 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
- [8] Pigmented Villonodular Synovitis in a Patient With Noonan Syndrome and SOS1 Gene MutationAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (22) : 2966 - 2967Mascheroni, Elisabetta论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, Rheumatol Unit, I-00165 Rome, Italy Bambino Gesu Pediat Hosp, Med Genet Unit, I-00165 Rome, ItalyDigilio, M. Cristina论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, Med Genet Unit, I-00165 Rome, Italy Bambino Gesu Pediat Hosp, Med Genet Unit, I-00165 Rome, ItalyCortis, Elisabetta论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, Rheumatol Unit, I-00165 Rome, Italy Bambino Gesu Pediat Hosp, Med Genet Unit, I-00165 Rome, ItalyDevito, Rita论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, Dept Pathol, I-00165 Rome, Italy Bambino Gesu Pediat Hosp, Med Genet Unit, I-00165 Rome, ItalySarkozy, Anna论文数: 0 引用数: 0 h-index: 0机构: Univ Roma La Sapienza, CSS Mendel Inst, Rome, Italy Bambino Gesu Pediat Hosp, Med Genet Unit, I-00165 Rome, ItalyCapolino, Rossella论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, Med Genet Unit, I-00165 Rome, Italy Bambino Gesu Pediat Hosp, Med Genet Unit, I-00165 Rome, ItalyDallapiccola, Bruno论文数: 0 引用数: 0 h-index: 0机构: Univ Roma La Sapienza, CSS Mendel Inst, Rome, Italy Bambino Gesu Pediat Hosp, Med Genet Unit, I-00165 Rome, ItalyUgazio, Alberto G.论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, Rheumatol Unit, I-00165 Rome, Italy Bambino Gesu Pediat Hosp, Med Genet Unit, I-00165 Rome, Italy
- [9] Germline gain-of-function mutations in SOS1 cause Noonan syndromeNATURE GENETICS, 2007, 39 (01) : 70 - 74Roberts, Amy E.论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USAAraki, Toshiyuki论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USASwanson, Kenneth D.论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USAMontgomery, Kate T.论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USASchiripo, Taryn A.论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USAJoshi, Victoria A.论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USALi, Li论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USAYassin, Yosuf论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USATamburino, Alex M.论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USANeel, Benjamin G.论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USA Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USAKucherlapati, Raju S.论文数: 0 引用数: 0 h-index: 0机构: Beth Israel Deaconess Med Ctr, Canc Biol Program, Div Hematol Oncol, Dept Med, Boston, MA 02115 USA
- [10] Tumor Spectrum in Children With Noonan Syndrome and SOS1 or RAF1 MutationsGENES 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