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- [21] A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disabilityELIFE, 2018, 7Chia, Poh Hui论文数: 0 引用数: 0 h-index: 0机构: Immunos, Inst Med Biol, Singapore, Singapore Immunos, Inst Med Biol, Singapore, SingaporeZhong, Franklin Lei论文数: 0 引用数: 0 h-index: 0机构: Immunos, Inst Med Biol, Singapore, Singapore Inst Mol & Cell Biol, Proteos, Singapore Immunos, Inst Med Biol, Singapore, SingaporeNiwa, Shinsuke论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Frontier Res Inst Interdisciplinary Sci, Sendai, Miyagi, Japan Tohoku Univ, Grad Sch Life Sci, Sendai, Miyagi, Japan Immunos, Inst Med Biol, Singapore, SingaporeBonnard, Carine论文数: 0 引用数: 0 h-index: 0机构: Immunos, Inst Med Biol, Singapore, Singapore Immunos, Inst Med Biol, Singapore, SingaporeUtami, Kagistia Hana论文数: 0 引用数: 0 h-index: 0机构: Agcy Sci Technol & Res, Translat Lab Genet Med, Singapore, Singapore Immunos, Inst Med Biol, Singapore, SingaporeZhang, Ruizhu论文数: 0 引用数: 0 h-index: 0机构: Agcy Sci Technol & Res, Translat Lab Genet Med, Singapore, Singapore Immunos, Inst Med Biol, Singapore, SingaporeLee, Hane论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Immunos, Inst Med Biol, Singapore, SingaporeEskin, Ascia论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Immunos, Inst Med Biol, Singapore, SingaporeNelson, Stanley F.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Immunos, Inst Med Biol, Singapore, SingaporeXie, William H.论文数: 0 引用数: 0 h-index: 0机构: Immunos, Inst Med Biol, Singapore, Singapore Immunos, Inst Med Biol, Singapore, SingaporeAl-Tawalbeh, Samah论文数: 0 引用数: 0 h-index: 0机构: Queen Rania Paediat Hosp, Kin Hussein Med Ctr, Royal Med Serv, Amman, Jordan Immunos, Inst Med Biol, Singapore, SingaporeEl-Khateeb, Mohammad论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Diabet Endocrinol & Genet, Amman, Jordan Immunos, Inst Med Biol, Singapore, SingaporeShboul, Mohammad论文数: 0 引用数: 0 h-index: 0机构: Al Balqa Appl Univ, Fac Sci, Al Salt, Jordan Immunos, Inst Med Biol, Singapore, SingaporePouladi, Mahmoud A.论文数: 0 引用数: 0 h-index: 0机构: Agcy Sci Technol & Res, Translat Lab Genet Med, Singapore, Singapore Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Med, Singapore, Singapore Immunos, Inst Med Biol, Singapore, SingaporeAl-Raqad, Mohammad论文数: 0 引用数: 0 h-index: 0机构: Queen Rania Paediat Hosp, Kin Hussein Med Ctr, Royal Med Serv, Amman, Jordan Immunos, Inst Med Biol, Singapore, SingaporeReversade, Bruno论文数: 0 引用数: 0 h-index: 0机构: Immunos, Inst Med Biol, Singapore, Singapore Inst Mol & Cell Biol, Proteos, Singapore Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pediat, Singapore, Singapore Koc Univ, Sch Med, Med Genet Dept, Istanbul, Turkey Immunos, Inst Med Biol, Singapore, Singapore
- [22] Loss-of-Function CNKSR2 Mutation Is a Likely Cause of Non-Syndromic X-Linked Intellectual DisabilityMOLECULAR SYNDROMOLOGY, 2011, 2 (02) : 60 - 63Houge, G.论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Ctr Med Genet & Mol Med, NO-5021 Bergen, Norway Univ Bergen, Dept Clin Med, Bergen, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, NO-5021 Bergen, NorwayRasmussen, I. H.论文数: 0 引用数: 0 h-index: 0机构: Stavanger Univ Hosp, Dept Child Neurol, Stavanger, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, NO-5021 Bergen, NorwayHovland, R.论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Ctr Med Genet & Mol Med, NO-5021 Bergen, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, NO-5021 Bergen, Norway
- [23] Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disabilityEuropean Journal of Human Genetics, 2021, 29 : 1663 - 1668Natja Haag论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyEne-Choo Tan论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyMatthias Begemann论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyLars Buschmann论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyFlorian Kraft论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyPetra Holschbach论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyAngeline H. M. Lai论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyMaggie Brett论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyGaneshwaran H. Mochida论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyStephanie DiTroia论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyLynn Pais论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyJennifer E. Neil论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyMuna Al-Saffar论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyLaila Bastaki论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyChristopher A. Walsh论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyIngo Kurth论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical FacultyCordula Knopp论文数: 0 引用数: 0 h-index: 0机构: RWTH Aachen University,Institute of Human Genetics, Medical Faculty
- [24] Biallelic loss-of-function mutations in WDR11 are associated with microcephaly and intellectual disabilityEUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 255 - 256Haag, Natja论文数: 0 引用数: 0 h-index: 0机构: Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, Germany Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyTan, Ene C.论文数: 0 引用数: 0 h-index: 0机构: KK Womens & Childrens Hosp, KK Res Ctr Genet Serv, Singapore, Singapore Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyBegemann, Matthias论文数: 0 引用数: 0 h-index: 0机构: Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, Germany Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyBuschmann, Lars论文数: 0 引用数: 0 h-index: 0机构: Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, Germany Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyHoschbach, Petra论文数: 0 引用数: 0 h-index: 0机构: Rhein Westfal TH Aachen, Med Fac, Div Neuropediat & Social Pediat, Dept Pediat, Aachen, Germany Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyLai, Angeline H. M.论文数: 0 引用数: 0 h-index: 0机构: KK Womens & Childrens Hosp, KK Res Ctr Genet Serv, Singapore, Singapore Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyBrett, Maggie论文数: 0 引用数: 0 h-index: 0机构: KK Womens & Childrens Hosp, KK Res Ctr Genet Serv, Singapore, Singapore Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyMochida, Ganeshwaran H.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA USA Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA Harvard Med Sch, Dept Neurol, Boston, MA 02115 USA Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyDiTroia, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Ctr Mendelian Genom, Program Med & Populat Genet, Cambridge, MA 02142 USA Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyPais, Lynn论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Ctr Mendelian Genom, Program Med & Populat Genet, Cambridge, MA 02142 USA Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyNail, Jennifer E.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA USA Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA Harvard Med Sch, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Howard Hughes Med Inst, Boston, MA USA Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyAl-Saffar, Muna论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA USA Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA Harvard Med Sch, Dept Neurol, Boston, MA 02115 USA United Arab Emirates Univ, Dept Paediat, Coll Med & Hlth Sci, Al Ain, U Arab Emirates Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyBastaki, Laila论文数: 0 引用数: 0 h-index: 0机构: Kuwait Med Genet Ctr, Matern Hosp, Kuwait, Kuwait Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyWalsh, Christopher A.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA USA Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA Harvard Med Sch, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Howard Hughes Med Inst, Boston, MA USA Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyKurth, Ingo论文数: 0 引用数: 0 h-index: 0机构: Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, Germany Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, GermanyKnopp, Cordula论文数: 0 引用数: 0 h-index: 0机构: Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, Germany Rhein Westfal TH Aachen, Inst Human Genet, Med Fac, Aachen, Germany
- [25] RSRCI loss-of-function variants cause mild to moderate autosomal recessive intellectual disabilityBRAIN, 2020, 143Scala, Marcello论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Queen Sq Inst Neurol, London, England Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Pediat Neurol & Muscular Dis Unit, Genoa, Italy UCL, UCL Queen Sq Inst Neurol, London, EnglandMojarrad, Majid论文数: 0 引用数: 0 h-index: 0机构: Mashhad Univ Med Sci, Dept Med Genet, Fac Med, Mashhad, Razavi Khorasan, Iran Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad, Razavi Khorasan, Iran Genet Ctr Khorasan Razavi, Mashhad, Razavi Khorasan, Iran UCL, UCL Queen Sq Inst Neurol, London, EnglandRiazuddin, Saima论文数: 0 引用数: 0 h-index: 0机构: Univ Maryland, Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Baltimore, MD 21201 USA UCL, UCL Queen Sq Inst Neurol, London, EnglandBrigatti, Karlla W.论文数: 0 引用数: 0 h-index: 0机构: Clin Special Children, Strasburg, PA USA UCL, UCL Queen Sq Inst Neurol, London, EnglandAmmous, Zineb论文数: 0 引用数: 0 h-index: 0机构: Community Hlth Clin, Topeka, IN USA UCL, UCL Queen Sq Inst Neurol, London, EnglandCohen, Julie S.论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Med Inst, Dept Neurol, Kennedy Krieger Inst, Baltimore, MD 21205 USA Johns Hopkins Med Inst, Dept Pediat, Kennedy Krieger Inst, Baltimore, MD 21205 USA UCL, UCL Queen Sq Inst Neurol, London, EnglandHosny, Heba论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neuromotor Syst, Cairo, Egypt UCL, UCL Queen Sq Inst Neurol, London, EnglandUsmani, Muhammad A.论文数: 0 引用数: 0 h-index: 0机构: Univ Maryland, Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Baltimore, MD 21201 USA UCL, UCL Queen Sq Inst Neurol, London, EnglandShahzad, Mohsin论文数: 0 引用数: 0 h-index: 0机构: Shaheed Zulfiqar Ali Bhutto Med Univ, Pakistan Inst Med Sci, Ctr Genet Dis, Islamabad, Pakistan UCL, UCL Queen Sq Inst Neurol, London, EnglandRiazuddin, Sheikh论文数: 0 引用数: 0 h-index: 0机构: Shaheed Zulfiqar Ali Bhutto Med Univ, Pakistan Inst Med Sci, Ctr Genet Dis, Islamabad, Pakistan Univ Punjab, Natl Ctr Excellence Mol Biol, Lahore 53700, Pakistan UCL, UCL Queen Sq Inst Neurol, London, EnglandStanley, Valentina论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Dept Neurosci, Rady Childrens Inst Genom Med, Howard Hughes Med Inst, San Diego, CA 92103 USA UCL, UCL Queen Sq Inst Neurol, London, EnglandEslahi, Atiye论文数: 0 引用数: 0 h-index: 0机构: Mashhad Univ Med Sci, Dept Med Genet, Fac Med, Mashhad, Razavi Khorasan, Iran Mashhad Univ Med Sci, Med Genet Res Ctr, Fac Med, Mashhad, Razavi Khorasan, Iran UCL, UCL Queen Sq Inst Neurol, London, EnglandPerson, Richard E.论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA UCL, UCL Queen Sq Inst Neurol, London, EnglandElbendary, Hasnaa M.论文数: 0 引用数: 0 h-index: 0机构: Natl Res Ctr, Human Genet & Genome Res Div, Clin Genet Dept, Cairo 12311, Egypt UCL, UCL Queen Sq Inst Neurol, London, EnglandComi, Anne M.论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Med Inst, Dept Neurol, Kennedy Krieger Inst, Baltimore, MD 21205 USA Johns Hopkins Med Inst, Dept Pediat, Kennedy Krieger Inst, Baltimore, MD 21205 USA UCL, UCL Queen Sq Inst Neurol, London, EnglandPoskitt, Laura论文数: 0 引用数: 0 h-index: 0机构: Clin Special Children, Strasburg, PA USA UCL, UCL Queen Sq Inst Neurol, London, EnglandSalpietro, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Queen Sq Inst Neurol, London, England Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Pediat Neurol & Muscular Dis Unit, Genoa, Italy UCL, UCL Queen Sq Inst Neurol, London, EnglandRosenfeld, Jill 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 UCL, UCL Queen Sq Inst Neurol, London, EnglandWilliams, Katie B.论文数: 0 引用数: 0 h-index: 0机构: Univ Wisconsin Hosp & Clin, Dept Pediat, Madison, WI 53792 USA UCL, UCL Queen Sq Inst Neurol, London, EnglandMarafi, Dana论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA UCL, UCL Queen Sq Inst Neurol, London, EnglandXia, Fan论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA UCL, UCL Queen Sq Inst Neurol, London, EnglandWaberski, Marta Biderman论文数: 0 引用数: 0 h-index: 0机构: NHGRI, Genet & Mol Biol Branch, NIH, Bethesda, MD 20892 USA UCL, UCL Queen Sq Inst Neurol, London, EnglandZaki, Maha S.论文数: 0 引用数: 0 h-index: 0机构: Natl Res Ctr, Human Genet & Genome Res Div, Clin Genet Dept, Cairo 12311, Egypt UCL, UCL Queen Sq Inst Neurol, London, EnglandGleeson, Joseph论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Dept Neurosci, Rady Childrens Inst Genom Med, Howard Hughes Med Inst, San Diego, CA 92103 USA UCL, UCL Queen Sq Inst Neurol, London, EnglandPuffenberger, Erik论文数: 0 引用数: 0 h-index: 0机构: Clin Special Children, Strasburg, PA USA UCL, UCL Queen Sq Inst Neurol, London, EnglandHoulden, Henry论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Queen Sq Inst Neurol, London, England UCL, UCL Queen Sq Inst Neurol, London, EnglandMaroofian, Reza论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Queen Sq Inst Neurol, London, England UCL, UCL Queen Sq Inst Neurol, London, England
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- [27] De novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disabilityAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (10) : 2231 - 2237Parker, Michael J.论文数: 0 引用数: 0 h-index: 0机构: Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, England Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, EnglandFryer, Alan E.论文数: 0 引用数: 0 h-index: 0机构: Alder Hey Childrens NHS Fdn Trust, Dept Clin Genet, Liverpool, Merseyside, England Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, EnglandShears, Deborah J.论文数: 0 引用数: 0 h-index: 0机构: Oxford Univ Hosp NHS Trust, Churchill Hosp, Dept Clin Genet, Oxford, England Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, EnglandLachlan, Katherine L.论文数: 0 引用数: 0 h-index: 0机构: Southampton Univ Hosp, Wessex Clin Genet Serv, Southampton, Hants, England Univ Southampton, Fac Med, Human Genet & Genom Med, Southampton SO9 5NH, Hants, England Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, EnglandMcKee, Shane A.论文数: 0 引用数: 0 h-index: 0机构: Belfast City Hosp, Dept Med Genet, Belfast BT9 7AD, Antrim, North Ireland Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, EnglandMagee, Alex C.论文数: 0 引用数: 0 h-index: 0机构: Belfast City Hosp, Dept Med Genet, Belfast BT9 7AD, Antrim, North Ireland Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, EnglandMohammed, Shehla论文数: 0 引用数: 0 h-index: 0机构: Guys & St Thomas Hosp NHS Trust, Dept Clin Genet, London, England Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, EnglandVasudevan, Pradeep C.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Leicester NHS Trust, Dept Clin Genet, Leicester Royal Infirm, Leicester, Leics, England Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, England论文数: 引用数: h-index:机构:Benoit, Valerie论文数: 0 引用数: 0 h-index: 0机构: Inst Pathol & Genet, Ctr Genet Humaine, Gosselies Charleroi, Belgium Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, EnglandLederer, Damien论文数: 0 引用数: 0 h-index: 0机构: Inst Pathol & Genet, Ctr Genet Humaine, Gosselies Charleroi, Belgium Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, EnglandMaystadt, Isabelle论文数: 0 引用数: 0 h-index: 0机构: Inst Pathol & Genet, Ctr Genet Humaine, Gosselies Charleroi, Belgium Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, EnglandFitzPatrick, David R.论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh EH8 9YL, Midlothian, Scotland Sheffield Childrens NHS Fdn Trust, Western Bank, Sheffield S10 2TH, S Yorkshire, England
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