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- [22] Identification of Two Novel Loss-of-Function SIM1 Mutations in Two Overweight Children with Developmental DelayOBESITY, 2014, 22 (12) : 2621 - 2624Montagne, Louise论文数: 0 引用数: 0 h-index: 0机构: European Genom Inst Diabet, Lille, France Lille Pasteur Inst, CNRS, UMR8199, Lille, France Univ Lille 2, Lille, France Catholic Univ Lille, St Vincent de Paul Hosp, St Antoine Pediat Hosp, Dept Pediat, Lille, France European Genom Inst Diabet, Lille, FranceRaimondo, Anne论文数: 0 引用数: 0 h-index: 0机构: Univ Adelaide, Sch Mol & Biomed Sci, Adelaide, SA, Australia Univ Adelaide, Australian Res Council, Special Res Ctr Mol Genet Dev, Adelaide, SA, Australia European Genom Inst Diabet, Lille, FranceDelobel, Bruno论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Lille, St Vincent de Paul Hosp, Dept Cytogenet Med Genet, Lille, France European Genom Inst Diabet, Lille, FranceDuban-Bedu, Benedicte论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Lille, St Vincent de Paul Hosp, Dept Cytogenet Med Genet, Lille, France European Genom Inst Diabet, Lille, FranceNoblet, Fanny Stutzmann论文数: 0 引用数: 0 h-index: 0机构: European Genom Inst Diabet, Lille, France Lille Pasteur Inst, CNRS, UMR8199, Lille, France Univ Lille 2, Lille, France European Genom Inst Diabet, Lille, FranceDechaume, Aurelie论文数: 0 引用数: 0 h-index: 0机构: European Genom Inst Diabet, Lille, France Lille Pasteur Inst, CNRS, UMR8199, Lille, France Univ Lille 2, Lille, France European Genom Inst Diabet, Lille, FranceBersten, David C.论文数: 0 引用数: 0 h-index: 0机构: Univ Adelaide, Sch Mol & Biomed Sci, Adelaide, SA, Australia Univ Adelaide, Australian Res Council, Special Res Ctr Mol Genet Dev, Adelaide, SA, Australia European Genom Inst Diabet, Lille, FranceMeyre, David论文数: 0 引用数: 0 h-index: 0机构: European Genom Inst Diabet, Lille, France Lille Pasteur Inst, CNRS, UMR8199, Lille, France Univ Lille 2, Lille, France McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON, Canada European Genom Inst Diabet, Lille, FranceWhitelaw, Murray L.论文数: 0 引用数: 0 h-index: 0机构: Univ Adelaide, Sch Mol & Biomed Sci, Adelaide, SA, Australia Univ Adelaide, Australian Res Council, Special Res Ctr Mol Genet Dev, Adelaide, SA, Australia European Genom Inst Diabet, Lille, FranceFroguel, Philippe论文数: 0 引用数: 0 h-index: 0机构: European Genom Inst Diabet, Lille, France Lille Pasteur Inst, CNRS, UMR8199, Lille, France Univ Lille 2, Lille, France Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, Dept Genom Common Dis, London, England European Genom Inst Diabet, Lille, FranceBonnefond, Amelie论文数: 0 引用数: 0 h-index: 0机构: European Genom Inst Diabet, Lille, France Lille Pasteur Inst, CNRS, UMR8199, Lille, France Univ Lille 2, Lille, France European Genom Inst Diabet, Lille, France
- [23] Arts syndrome is caused by loss-of-function mutations in PRPS1AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 81 (03) : 507 - 518de Brouwer, Arjan P. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsWilliams, Kelly L.论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsDuley, John A.论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsvan Kuilenburg, Andre B. P.论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsNabuurs, Sander B.论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsEgmont-Petersen, Michael论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsLugtenberg, Dorien论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsZoetekouw, Lida论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsBanning, Martijn J. G.论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsRoeffen, Melissa论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsHamel, Ben C. J.论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsWeaving, Linda论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsOuvrier, Robert A.论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsDonald, Jennifer A.论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsWevers, Ron A.论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsChristodoulou, John论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsvan Bokhoven, Hans论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen St Radboud Hosp, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
- [24] Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossHuman Genetics, 2020, 139 : 1565 - 1574Kevin T. Booth论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyAmama Ghaffar论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyMuhammad Rashid论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyLuke T. Hovey论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyMureed Hussain论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyKathy Frees论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyErika M. Renkes论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyCarla J. Nishimura论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyMohsin Shahzad论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyRichard J. Smith论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyZubair Ahmed论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyHela Azaiez论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologySaima Riazuddin论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology
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