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- [41] Bi-allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal AbnormalitiesAMERICAN JOURNAL OF HUMAN GENETICS, 2020, 107 (06) : 1044 - 1061Schneeberger, Pauline E.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germanyvon Elsner, Leonie论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, GermanyBarker, Emma L.论文数: 0 引用数: 0 h-index: 0机构: Univ Nottingham, Nottingham Biodiscovery Inst, Univ Pk, Nottingham NG7 2RD, England Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, GermanyMeinecke, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, GermanyMarquardt, Iris论文数: 0 引用数: 0 h-index: 0机构: Klinikum Oldenburg, Klin Neuropadiatrie & Angeborene Stoffwechselerkr, D-26133 Oldenburg, Germany Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, GermanyAlawi, Malik论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Bioinformat Core, D-20246 Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, GermanySteindl, Katharina论文数: 0 引用数: 0 h-index: 0机构: Univ Zurich, Inst Med Genet, CH-8952 Schlieren, Switzerland Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, GermanyJoset, Pascal论文数: 0 引用数: 0 h-index: 0机构: Univ Zurich, Inst Med Genet, CH-8952 Schlieren, Switzerland Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany论文数: 引用数: h-index:机构:Zwijnenburg, Petra J. G.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Dept Clin Genet, Med Ctr, NL-1081 Amsterdam, Netherlands Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, GermanyWeiss, Marjan M.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Dept Clin Genet, Med Ctr, NL-1081 Amsterdam, Netherlands Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, GermanyMerry, Catherine L. R.论文数: 0 引用数: 0 h-index: 0机构: Univ Nottingham, Nottingham Biodiscovery Inst, Univ Pk, Nottingham NG7 2RD, England Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, GermanyKutsche, Kerstin论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany
- [42] Bi-allelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with epilepsyNEUROLOGY, 2021, 96 (15)Calame, Daniel论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USABakhtiari, Somayeh论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Tucson, AZ 85721 USA Baylor Coll Med, Houston, TX 77030 USAMitani, Tadahiro论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USAFatih, Jawid论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USALogan, Rachel论文数: 0 引用数: 0 h-index: 0机构: Childrens Healthcare Atlanta, Atlanta, GA USA Baylor Coll Med, Houston, TX 77030 USAHunter, Jill论文数: 0 引用数: 0 h-index: 0机构: Texas Childrens Hosp, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USAHerman, Isabella论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USAPehlivan, Davut论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USAPosey, Jennifer论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USAZaki, Maha论文数: 0 引用数: 0 h-index: 0机构: Natl Res Ctr, Giza, Egypt Baylor Coll Med, Houston, TX 77030 USAMarafie, Dana论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USA论文数: 引用数: h-index:机构:Lupski, James论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USA
- [43] Bi-allelic variants in INSL3 and RXFP2 cause bilateral cryptorchidism and male infertilityHUMAN REPRODUCTION, 2023, 38 (07) : 1412 - 1423Dicke, Ann-Kristin论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, Germany Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyAlbrethsen, Jakob论文数: 0 引用数: 0 h-index: 0机构: Copenhagen Univ Hosp, Dept Growth & Reprod, Rigshosp, Copenhagen, Denmark Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyHoare, Bradley L.论文数: 0 引用数: 0 h-index: 0机构: Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyWyrwoll, Margot J.论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, Germany Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyBusch, Alexander S.论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp Munster, Dept Gen Paediat, Munster, Germany Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyFietz, Daniela论文数: 0 引用数: 0 h-index: 0机构: Justus Liebig Univ Giessen, Inst Vet Anat Histol & Embryol, Giessen, Germany Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyPilatz, Adrian论文数: 0 引用数: 0 h-index: 0机构: Justus Liebig Univ Giessen, Clin Urol Paediat Urol & Androl, Giessen, Germany Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyBuehlmann, Clara论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyJuul, Anders论文数: 0 引用数: 0 h-index: 0机构: Copenhagen Univ Hosp, Dept Growth & Reprod, Rigshosp, Copenhagen, Denmark Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyKliesch, Sabine论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Ctr Reprod Med & Androl, Munster, Germany Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyGromoll, Joerg论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Ctr Reprod Med & Androl, Munster, Germany Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyBathgate, Ross A. D.论文数: 0 引用数: 0 h-index: 0机构: Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia Univ Melbourne, Dept Biochem & Pharmacol, Melbourne, Vic, Australia Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyTuettelmann, Frank论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, Germany Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, GermanyStallmeyer, Birgit论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, Germany Univ Munster, Inst Reprod Genet, Vesaliusweg 12-14, D-48149 Munster, Germany
- [44] Bi-allelic variants in INSL3 and RXFP2 cause bilateral cryptorchidism and male infertilityEUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 346 - 346Dicke, Ann-Kristin论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Reprod Genet, Munster, Germany Univ Munster, Inst Reprod Genet, Munster, GermanyWyrwoll, Margot Julia论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Reprod Genet, Munster, Germany Univ Munster, Inst Reprod Genet, Munster, GermanyAlbrethsen, Jakob Christian论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Reprod Genet, Munster, GermanyBusch, Alexander论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Dept Growth & Reprod, Rigshosp, Copenhagen, Denmark Univ Munster, Inst Reprod Genet, Munster, GermanyFietz, D.论文数: 0 引用数: 0 h-index: 0机构: Justus Liebig Univ Giessen, Inst Vet Anat Histol & Embryol, Giessen, Germany Univ Munster, Inst Reprod Genet, Munster, GermanyPilatz, Adrian论文数: 0 引用数: 0 h-index: 0机构: Justus Liebig Univ Giessen, Clin Urol Paediat Urol & Androl, Giessen, Germany Univ Munster, Inst Reprod Genet, Munster, GermanyJuul, Anders论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Dept Growth & Reprod, Rigshosp, Copenhagen, Denmark Univ Munster, Inst Reprod Genet, Munster, GermanyKliesch, Sabine论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Munster, Ctr Reprod Med & Androl, Munster, Germany Univ Munster, Inst Reprod Genet, Munster, GermanyGromoll, Joerg论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Munster, Ctr Reprod Med & Androl, Munster, Germany Univ Munster, Inst Reprod Genet, Munster, GermanyStallmeyer, Birgit论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Reprod Genet, Munster, Germany Univ Munster, Inst Reprod Genet, Munster, GermanyTuettelmann, Frank论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Reprod Genet, Munster, Germany Univ Munster, Inst Reprod Genet, Munster, Germany
- [45] Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac AbnormalitiesAMERICAN JOURNAL OF HUMAN GENETICS, 2020, 106 (05) : 623 - 631Muir, Alison M.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USACohen, Jennifer L.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Duke Univ, Dept Pediat, Sch Med, Div Med Genet, Durham, NC USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USASheppard, Sarah E.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USAGuttipatti, Pavithran论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Raymond G Perelman Ctr Cellular & Mol Therapeut, Philadelphia, PA 19104 USA Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USALo, Tsz Y.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Raymond G Perelman Ctr Cellular & Mol Therapeut, Philadelphia, PA 19104 USA Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USAWeed, Natalie论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USA论文数: 引用数: h-index:机构:DeMarzo, Danielle论文数: 0 引用数: 0 h-index: 0机构: Univ Oklahoma, Dept Pediat, Oklahoma City, OK 73104 USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USAFagerberg, Christina R.论文数: 0 引用数: 0 h-index: 0机构: Odense Univ Hosp, Dept Clin Genet, Odense, Denmark Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USAKjaersgaard, Lars论文数: 0 引用数: 0 h-index: 0机构: Odense Univ Hosp, Hans Christian Andersen Childrens Hosp, Odense, Denmark Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USALarsen, Martin J.论文数: 0 引用数: 0 h-index: 0机构: Odense Univ Hosp, Dept Clin Genet, Odense, Denmark Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USA论文数: 引用数: h-index:机构:Lohner, Katharina论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USAHirsch, Yoel论文数: 0 引用数: 0 h-index: 0机构: Comm Prevent Jewish Genet Dis, Jerusalem, Israel Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USAZeevi, David A.论文数: 0 引用数: 0 h-index: 0机构: Comm Prevent Jewish Genet Dis, Jerusalem, Israel Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USAZackai, Elaine H.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USABhoj, Elizabeth论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USASong, Yuanquan论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Raymond G Perelman Ctr Cellular & Mol Therapeut, Philadelphia, PA 19104 USA Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USAMefford, Heather C.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USA Seattle Childrens Hosp, Seattle, WA 98105 USA Brotman Baty Inst Precis Med, Seattle, WA 98195 USA Univ Washington, Dept Pediat, Div Genet Med, Seattle, WA 98195 USA
- [46] Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulationAMERICAN JOURNAL OF HUMAN GENETICS, 2021, 108 (06) : 1126 - 1137论文数: 引用数: h-index:机构:Duclaux-Loras, Remi论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Imagine Inst, Lab Intestinal Immun, INSERM,UMR1163, F-75015 Paris, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceRevenu, Celine论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, INSERM, Inst Vis, CNRS, 17 Rue Moreau, F-75012 Paris, France PSL Res Univ, Inst Curie, INSERM U934, CNRS UMR3215, F-75005 Paris, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceCharbit-Henrion, Fabienne论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Imagine Inst, Lab Intestinal Immun, INSERM,UMR1163, F-75015 Paris, France Hop Necker Enfants Malad, AP HP, Dept Pediat Gastroenterol, F-75015 Paris, France Hop Necker Enfants Malad, AP HP, Dept Mol Genet, F-75015 Paris, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, France论文数: 引用数: h-index:机构:Duroure, Karine论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, INSERM, Inst Vis, CNRS, 17 Rue Moreau, F-75012 Paris, France PSL Res Univ, Inst Curie, INSERM U934, CNRS UMR3215, F-75005 Paris, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceGrimaud, Linda论文数: 0 引用数: 0 h-index: 0机构: Univ Angers, MitoVasc, INSERM 1083, UMR CNRS 6015, F-49933 Angers, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceGuihot, Anne Laure论文数: 0 引用数: 0 h-index: 0机构: Univ Angers, MitoVasc, INSERM 1083, UMR CNRS 6015, F-49933 Angers, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceDesquiret-Dumas, Valerie论文数: 0 引用数: 0 h-index: 0机构: CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, France Univ Angers, MitoVasc, INSERM 1083, UMR CNRS 6015, F-49933 Angers, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceZarhrate, Mohammed论文数: 0 引用数: 0 h-index: 0机构: Paris Descartes Sorbonne Paris Cite Univ, INSERM U1163, Inst Imagine Struct Federat Rech Necker, Genom Core Facil, F-75015 Paris, France Paris Descartes Sorbonne Paris Cite Univ, INSERM US24, CNRS UMS3633, F-75015 Paris, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceCagnard, Nicolas论文数: 0 引用数: 0 h-index: 0机构: Imagine Inst, INSERM UMR 1163, Bioinformat Core Facil, F-75015 Paris, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceMas, Emmanuel论文数: 0 引用数: 0 h-index: 0机构: Univ Toulouse, ENVT, INRA, INSERM,UPS,IRSD, F-31300 Toulouse, France CHU Toulouse, Toulouse Clin Invest Ctr INSERM U1436, Hop Enfants, Ctr Reference Malad Rares Digest, F-31300 Toulouse, France CHU Toulouse, Toulouse Clin Invest Ctr INSERM U1436, Hop Enfants, Pediat Clin Res Unit, F-31300 Toulouse, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceBreton, Anne论文数: 0 引用数: 0 h-index: 0机构: Univ Toulouse, ENVT, INRA, INSERM,UPS,IRSD, F-31300 Toulouse, France CHU Toulouse, Toulouse Clin Invest Ctr INSERM U1436, Hop Enfants, Ctr Reference Malad Rares Digest, F-31300 Toulouse, France CHU Toulouse, Toulouse Clin Invest Ctr INSERM U1436, Hop Enfants, Pediat Clin Res Unit, F-31300 Toulouse, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, France论文数: 引用数: h-index:机构:Billon, Clarisse论文数: 0 引用数: 0 h-index: 0机构: Hop Europeen Georges Pompidou, AP HP, Ctr Reference Malad Vasculaires Rares, Ctr Genet, F-75015 Paris, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceFrank, Michael论文数: 0 引用数: 0 h-index: 0机构: Hop Europeen Georges Pompidou, AP HP, Ctr Reference Malad Vasculaires Rares, Ctr Genet, F-75015 Paris, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceColin, Estelle论文数: 0 引用数: 0 h-index: 0机构: CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceLenaers, Guy论文数: 0 引用数: 0 h-index: 0机构: Univ Angers, MitoVasc, INSERM 1083, UMR CNRS 6015, F-49933 Angers, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceHenrion, Daniel论文数: 0 引用数: 0 h-index: 0机构: Univ Angers, MitoVasc, INSERM 1083, UMR CNRS 6015, F-49933 Angers, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceLyonnet, Stanislas论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Lab Embryol & Genet Malformat, Imagine Inst, INSERM UMR 1163, F-75015 Paris, France Hop Necker Enfants Malad, AP HP, Federat Genet, F-75015 Paris, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceFaivre, Laurence论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, Ctr Reference Anomalies Dev & Syndromes Malformat, Hop Enfants, FHU TRANSLAD, F-21000 Dijon, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceAlembik, Yves论文数: 0 引用数: 0 h-index: 0机构: CHU Hautepierre, Dept Genet Med, F-67200 Strasbourg, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FrancePhilippe, Anais论文数: 0 引用数: 0 h-index: 0机构: CHU Hautepierre, Dept Genet Med, F-67200 Strasbourg, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceMoulin, Bruno论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Nouvel Hop Civil, Nephrol & Transplantat Dept, F-67200 Strasbourg, France CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceReinstein, Eyal论文数: 0 引用数: 0 h-index: 0机构: Meir Med Ctr, Med Genet Inst, IL-4428164 Kefar Sava, Israel Tel Aviv Univ, Sackler Fac Med, IL-6997801 Tel Aviv, Israel CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceTzur, Shay论文数: 0 引用数: 0 h-index: 0机构: Genom Res Dept, Emedgene Technol, IL-67443 Tel Aviv, Israel CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceAttali, Ruben论文数: 0 引用数: 0 h-index: 0机构: Genom Res Dept, Emedgene Technol, IL-67443 Tel Aviv, Israel CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceMcGillivray, George论文数: 0 引用数: 0 h-index: 0机构: Murdoch Childrens Res Inst, Victorian Clin Genet Serv, Melbourne, Vic 3052, Australia CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceWhite, Susan M.论文数: 0 引用数: 0 h-index: 0机构: Murdoch Childrens Res Inst, Victorian Clin Genet Serv, Melbourne, Vic 3052, Australia CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceGallacher, Lyndon论文数: 0 引用数: 0 h-index: 0机构: Murdoch Childrens Res Inst, Victorian Clin Genet Serv, Melbourne, Vic 3052, Australia Univ Melbourne, Dept Paediat, Melbourne, Vic 3010, Australia CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceKutsche, Kerstin论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceSchneeberger, Pauline论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceGirisha, Katta M.论文数: 0 引用数: 0 h-index: 0机构: Manipal Acad Higher Educ, Kasturba Med Coll, Dept Med Genet, Manipal 576104, India CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceNayak, Shalini S.论文数: 0 引用数: 0 h-index: 0机构: Manipal Acad Higher Educ, Kasturba Med Coll, Dept Med Genet, Manipal 576104, India CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FrancePais, Lynn论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Broad Ctr Mendelian Genom, Program Med & Populat Genet, Cambridge, MA 02142 USA CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceMaroofian, Reza论文数: 0 引用数: 0 h-index: 0机构: UCL, Dept Neuromuscular Disorders, Queen Sq Inst Neurol, London WC1N 3BG, England CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceRad, Aboulfazl论文数: 0 引用数: 0 h-index: 0机构: Eberhard Karls Univ Tubingen, Tubingen Hearing Res Ctr, Dept Otolaryngol Head & Neck Surg, D-72076 Tubingen, Germany CHU Angers, Dept Biochem & Mol Biol, F-49933 Angers, FranceVona, Barbara论文数: 0 引用数: 0 h-index: 0机构: Eberhard Karls Univ Tubingen, Tubingen Hearing Res Ctr, Dept Otolaryngol Head & Neck Surg, D-72076 Tubingen, Germany Julius Maximilians Univ Wurzburg, Inst Human Genet, D-97074 Wurzburg, Germany CHU Angers, Dept Biochem & Mol Biol, 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