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- [1] Genotype-Phenotype Correlations in VHL Exon DeletionsAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2009, 149A (10) : 2147 - 2151McNeill, Alisdair论文数: 0 引用数: 0 h-index: 0机构: Univ Birmingham, Inst Biomed Res, Dept Med & Mol Genet, Birmingham B15 2TT, W Midlands, England Birmingham Womens Hosp, W Midlands Reg Genet Serv, Birmingham, W Midlands, England Univ Birmingham, Inst Biomed Res, Dept Med & Mol Genet, Birmingham B15 2TT, W Midlands, EnglandRattenberry, Eleanor论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp, W Midlands Reg Genet Serv, Birmingham, W Midlands, England Univ Birmingham, Inst Biomed Res, Dept Med & Mol Genet, Birmingham B15 2TT, W Midlands, EnglandBarber, Richard论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp, W Midlands Reg Genet Serv, Birmingham, W Midlands, England Univ Birmingham, Inst Biomed Res, Dept Med & Mol Genet, Birmingham B15 2TT, W Midlands, EnglandKillick, Pip论文数: 0 引用数: 0 h-index: 0机构: Univ Birmingham, Inst Biomed Res, Dept Med & Mol Genet, Birmingham B15 2TT, W Midlands, England Univ Birmingham, Inst Biomed Res, Dept Med & Mol Genet, Birmingham B15 2TT, W Midlands, EnglandMacDonald, Fiona论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp, W Midlands Reg Genet Serv, Birmingham, W Midlands, England Univ Birmingham, Inst Biomed Res, Dept Med & Mol Genet, Birmingham B15 2TT, W Midlands, EnglandMaher, Eamonn R.论文数: 0 引用数: 0 h-index: 0机构: Univ Birmingham, Inst Biomed Res, Dept Med & Mol Genet, Birmingham B15 2TT, W Midlands, England Birmingham Womens Hosp, W Midlands Reg Genet Serv, Birmingham, W Midlands, England Univ Birmingham, Inst Biomed Res, Dept Med & Mol Genet, Birmingham B15 2TT, W Midlands, England
- [2] Genotype-phenotype correlations in families with deletions in the von Hippel-Lindau (VHL) geneHuman Genetics, 2000, 106 : 425 - 431Frederik Hes论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Richard Zewald论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Ton Peeters论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Rolf Sijmons论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Thera Links论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Joke Verheij论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Gert Matthijs论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Eric Legius论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Geert Mortier论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Kors van der Torren论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Malou Rosman论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Cornelis Lips论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Peter Pearson论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,Rob van der Luijt论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics,
- [3] Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletionsEUROPEAN JOURNAL OF HUMAN GENETICS, 2012, 20 (12) : 1240 - 1247Schaaf, Christian P.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USABoone, Philip M.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USASampath, Srirangan论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAWilliams, Charles论文数: 0 引用数: 0 h-index: 0机构: Univ Florida, Dept Pediat, Div Genet & Metab, Gainesville, FL USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USABader, Patricia I.论文数: 0 引用数: 0 h-index: 0机构: Genet Ctr, Parkview Hlth Labs, Ft Wayne, IN USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAMueller, Jennifer M.论文数: 0 引用数: 0 h-index: 0机构: Univ Florida, Dept Pediat, Div Genet & Metab, Gainesville, FL USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAShchelochkov, Oleg A.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa Hosp & Clin, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USABrown, Chester W.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USACrawford, Heather P.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAPhalen, James A.论文数: 0 引用数: 0 h-index: 0机构: USAF, Dev Pediat Serv, San Antonio Mil Med Ctr, Lackland AFB, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USATartaglia, Nicole R.论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Denver Sch Med, Dept Pediat, Aurora, CO USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAEvans, Patricia论文数: 0 引用数: 0 h-index: 0机构: Univ Texas SW, Div Pediat Neurol, Dept Pediat, Dallas, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USACampbell, William M.论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Denver Sch Med, Dept Pediat, Aurora, CO USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USATsai, Anne Chun-Hui论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Denver Sch Med, Dept Pediat, Aurora, CO USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAParsley, Lea论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Denver Sch Med, Dept Pediat, Aurora, CO USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAGrayson, Stephanie W.论文数: 0 引用数: 0 h-index: 0机构: Kaiser Permanente, Lafayette, CO USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAScheuerle, Angela论文数: 0 引用数: 0 h-index: 0机构: Tesserae Genet, Dallas, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USALuzzi, Carol D.论文数: 0 引用数: 0 h-index: 0机构: Mem Behav & Dev Pediat, South Bend, IN USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAThomas, Sandra K.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hlth Ctr, Marble Falls, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAEng, Patricia A.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAKang, Sung-Hae L.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAPatel, Ankita论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAStankiewicz, Pawel论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Inst Mother & Child Hlth, Dept Med Genet, Warsaw, Poland Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USACheung, Sau W.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
- [4] Genotype-phenotype correlations in families with deletions in the von Hippel-Lindau (VHL) geneHUMAN GENETICS, 2000, 106 (04) : 425 - 431Hes, F论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsZewald, R论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsPeeters, T论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsSijmons, R论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsLinks, T论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsVerheij, J论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsMatthijs, G论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsLegius, E论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsMortier, G论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, Netherlandsvan der Torren, K论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsRosman, M论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsLips, C论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, NetherlandsPearson, P论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, Netherlandsvan der Luijt, R论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Ctr Med, Dept Med Genet, NL-3508 AB Utrecht, Netherlands
- [5] GENOTYPE-PHENOTYPE CORRELATIONS IN VONHIPPEL-LINDAU (VHL)-DISEASEJOURNAL OF MEDICAL GENETICS, 1995, 32 (02) : 137 - 138CROSSEY, PA论文数: 0 引用数: 0 h-index: 0机构: MEM UNIV NEWFOUNDLAND,DIV COMMUNITY MED,ST JOHNS,NF,CANADARICHARDS, FM论文数: 0 引用数: 0 h-index: 0机构: MEM UNIV NEWFOUNDLAND,DIV COMMUNITY MED,ST JOHNS,NF,CANADAGREEN, JS论文数: 0 引用数: 0 h-index: 0机构: MEM UNIV NEWFOUNDLAND,DIV COMMUNITY MED,ST JOHNS,NF,CANADANEUMANN, HPH论文数: 0 引用数: 0 h-index: 0机构: MEM UNIV NEWFOUNDLAND,DIV COMMUNITY MED,ST JOHNS,NF,CANADAFOSTER, K论文数: 0 引用数: 0 h-index: 0机构: MEM UNIV NEWFOUNDLAND,DIV COMMUNITY MED,ST JOHNS,NF,CANADAPROWSE, A论文数: 0 引用数: 0 h-index: 0机构: MEM UNIV NEWFOUNDLAND,DIV COMMUNITY MED,ST JOHNS,NF,CANADAAFFARA, NA论文数: 0 引用数: 0 h-index: 0机构: MEM UNIV NEWFOUNDLAND,DIV COMMUNITY MED,ST JOHNS,NF,CANADAFERGUSONSMITH, MA论文数: 0 引用数: 0 h-index: 0机构: MEM UNIV NEWFOUNDLAND,DIV COMMUNITY MED,ST JOHNS,NF,CANADAMAHER, ER论文数: 0 引用数: 0 h-index: 0机构: MEM UNIV NEWFOUNDLAND,DIV COMMUNITY MED,ST JOHNS,NF,CANADA
- [6] Alu-Alu Recombination Underlies the Vast Majority of Large VHL Germline Deletions: Molecular Characterization and Genotype-Phenotype Correlations in VHL PatientsHUMAN MUTATION, 2009, 30 (05) : 776 - 786Franke, Gerlind论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, Germany Univ Freiburg, Fac Biol, Freiburg, Germany Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, GermanyBausch, Birke论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, Germany Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, GermanyHoffmann, Michael M.论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Dept Lab Med, Freiburg, Germany Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, GermanyCybulla, Markus论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, Germany Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, GermanyWilhelm, Christian论文数: 0 引用数: 0 h-index: 0机构: Ctr Human Genet, Freiburg, Germany Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, GermanyKohlhase, Juergen论文数: 0 引用数: 0 h-index: 0机构: Ctr Human Genet, Freiburg, Germany Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, GermanyScherer, Gerd论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Human Genet & Anthropol, Freiburg, Germany Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, GermanyNeumann, Hartmut P. H.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, Germany Univ Med Ctr Freiburg, Dept Nephrol, Freiburg, Germany
- [7] Genotype-phenotype correlationsARRHYTHMOGENIC RV CARDIOMYOPATHY/ DYSPLASIA: RECENT ADVANCES, 2007, : 21 - +Bauce, Barbara论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Cardiol Thorac & Vasc Sci, Padua, Italy Univ Padua, Dept Cardiol Thorac & Vasc Sci, Padua, ItalyNava, Andrea论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Cardiol Thorac & Vasc Sci, Padua, Italy Univ Padua, Dept Cardiol Thorac & Vasc Sci, Padua, Italy
- [8] Genotype-phenotype correlations in two large deletions 13qCHROMOSOME RESEARCH, 2009, 17 : 82 - 83Tosca, L.论文数: 0 引用数: 0 h-index: 0机构: Hop Antoine Beclere, AP HP, F-92140 Clamart, France INSERM, U935, F-94801 Villejuif, France Hop Antoine Beclere, AP HP, F-92140 Clamart, FranceLatour, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Antoine Beclere, AP HP, F-92140 Clamart, France Hop Antoine Beclere, AP HP, F-92140 Clamart, FranceMetay, C.论文数: 0 引用数: 0 h-index: 0机构: Hop Henri Mondor, APHP, Plateforme Genom IMRB 955, F-94010 Creteil, France Hop Antoine Beclere, AP HP, F-92140 Clamart, FranceGuerin, N.论文数: 0 引用数: 0 h-index: 0机构: Hop Antoine Beclere, AP HP, F-92140 Clamart, France Hop Antoine Beclere, AP HP, F-92140 Clamart, FranceToujani, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Antoine Beclere, AP HP, F-92140 Clamart, France Hop Antoine Beclere, AP HP, F-92140 Clamart, FranceLebas, A.论文数: 0 引用数: 0 h-index: 0机构: Hop Bicetre, AP HP, F-94275 Le Kremlin Bicetre, France Hop Antoine Beclere, AP HP, F-92140 Clamart, FranceSenat, M., V论文数: 0 引用数: 0 h-index: 0机构: Hop Antoine Beclere, AP HP, F-92140 Clamart, France Hop Antoine Beclere, AP HP, F-92140 Clamart, FranceGoossens, M.论文数: 0 引用数: 0 h-index: 0机构: Hop Henri Mondor, APHP, Plateforme Genom IMRB 955, F-94010 Creteil, France Hop Antoine Beclere, AP HP, F-92140 Clamart, France论文数: 引用数: h-index:机构:Brisset, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Antoine Beclere, AP HP, F-92140 Clamart, France Univ Paris Sud, F-94276 Le Kremlin Bicetre, France INSERM, U782, F-92140 Clamart, France Hop Antoine Beclere, AP HP, F-92140 Clamart, France
- [9] Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletionsEuropean Journal of Human Genetics, 2012, 20 : 1240 - 1247Christian P Schaaf论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsPhilip M Boone论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsSrirangan Sampath论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsCharles Williams论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsPatricia I Bader论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsJennifer M Mueller论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsOleg A Shchelochkov论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsChester W Brown论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsHeather P Crawford论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsJames A Phalen论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsNicole R Tartaglia论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsPatricia Evans论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsWilliam M Campbell论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsAnne Chun-Hui Tsai论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsLea Parsley论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsStephanie W Grayson论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsAngela Scheuerle论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsCarol D Luzzi论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsSandra K Thomas论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsPatricia A Eng论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsSung-Hae L Kang论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsAnkita Patel论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsPawel Stankiewicz论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human GeneticsSau W Cheung论文数: 0 引用数: 0 h-index: 0机构: Baylor College of Medicine,Department of Molecular and Human Genetics
- [10] Genotype-phenotype correlations in retinoblastomaEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 588 - 589Le Gall, Jessica论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, FranceMahmoudi, Meriam论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, FranceMezghani, Sarah论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Imaging, Paris, France Inst Curie Hosp, Genet, Paris, FranceBouchoucha, Yassine论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Pediat, Paris, France Inst Curie Hosp, Genet, Paris, FranceMatet, Alexandre论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Paris, France Inst Curie Hosp, Ocular Oncol, Paris, France Inst Curie Hosp, Genet, Paris, FranceCardoen, Liesbeth论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Imaging, Paris, France Inst Curie Hosp, Genet, Paris, FranceGhazelian, Hrant论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, FranceCarriere, Jennifer论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, FranceFort, Nicolas论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, FranceGauthier-Villars, Marion论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, FranceStoppa-Lyonnet, Dominique论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France Univ Paris Cite, Paris, France Inst Curie Hosp, Genet, Paris, FranceHua, Clement论文数: 0 引用数: 0 h-index: 0机构: PSL Res Univ, Paris, France Inst Curie Hosp, Mol Oncol Team, Paris, France Inst Curie Hosp, Genet, Paris, FranceRadvanyi, Francois论文数: 0 引用数: 0 h-index: 0机构: PSL Res Univ, Paris, France Inst Curie Hosp, Mol Oncol Team, Paris, France Inst Curie Hosp, Genet, Paris, FranceFreneaux, Paul论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Biopathol, Paris, France Inst Curie Hosp, Genet, Paris, FranceBrisse, Herve论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Imaging, Paris, France Inst Curie Hosp, Genet, Paris, FranceCassoux, Nathalie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Paris, France Inst Curie Hosp, Ocular Oncol, Paris, France Inst Curie Hosp, Genet, Paris, FranceDoz, Francois论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Pediat, Paris, France Univ Paris Cite, Paris, France Inst Curie Hosp, Genet, Paris, FranceLisa, Golmard论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, France