机译:De Novo TBR1变体导致具有ID和自闭症的神经认知表型:举报25个新个人和文献审查
CHU Dijon Bourgogne Hop Enfants Ctr Genet Dijon France;
CHU Dijon Bourgogne Hop Enfants Ctr Genet Dijon France;
Seattle Childrens Res Inst Ctr Integrat Brain Res Seattle WA USA;
CHU Dijon Bourgogne Hop Enfants Ctr Genet Dijon France;
CHU Dijon Bourgogne Hop Enfants Ctr Genet Dijon France;
CHU Dijon Bourgogne Hop Enfants Ctr Genet Dijon France;
CHU Dijon Bourgogne Hop Enfants Ctr Genet Dijon France;
CHU Rouen Ctr Normand Genom Med &
Med Personnalisee Serv Genet Rouen France;
CHU Rouen Ctr Normand Genom Med &
Med Personnalisee Serv Genet Rouen France;
CHU Rouen Normandie Serv Pediat Rouen France;
Hop Trousseau Serv Genet &
Embryol Med Paris France;
CHU Lille Hop Jeanne Flandre Clin Genet Guy Fontaine Pole Biol Pathol Genet F-59000 Lille;
Hosp Civils Lyon Serv Genet Ctr Rech Neurosci Lyon INSERM U1028 CNRS UMR5292 GENDEVTeam Bron;
Hop Kremlin Bicetre Serv Neurol Pediat Paris France;
Grp Hosp Havre Serv Genet Le Havre France;
CHIC Creteil Unite Genet Med Creteil France;
CHU Lille Hop Jeanne Flandre Clin Genet Guy Fontaine Pole Biol Pathol Genet F-59000 Lille;
Childrens Hosp Philadelphia Dept Genet Philadelphia PA 19104 USA;
Mayo Clin Ctr Individualized Med Rochester MN 55905 USA;
Mayo Clin Ctr Individualized Med Rochester MN 55905 USA;
Mayo Clin Ctr Individualized Med Rochester MN 55905 USA;
Mayo Clin Ctr Individualized Med Rochester MN 55905 USA;
Washington Univ Sch Med Dept Pediat St Louis MO 63110 USA;
Washington Univ Sch Med Dept Pediat Div Genet &
Genom Med St Louis MO 63110 USA;
North York Gen Hosp Genet Program Toronto ON Canada;
HudsonAlpha Inst Biotechnol 601 Genome Way Huntsville AL USA;
HudsonAlpha Inst Biotechnol 601 Genome Way Huntsville AL USA;
Univ Hosp Leuven Ctr Dev Disorders Leuven Belgium;
Barbara Bush Childrens Hosp Maine Med Ctr Dept Pediat Portland OR USA;
Barbara Bush Childrens Hosp Maine Med Ctr Dept Pediat Portland OR USA;
Univ British Columbia Dept Med Genet Vancouver BC V6H 3N1 Canada;
Univ British Columbia Dept Med Genet Vancouver BC V6H 3N1 Canada;
CHU Nantes Serv Genet Med Nantes France;
Univ British Columbia Dept Med Genet Vancouver BC V6H 3N1 Canada;
CHU Nantes Serv Genet Med Nantes France;
Univ Florence Childrens Hosp Meyer Neurosci Dept Florence Italy;
Univ Florence Childrens Hosp Meyer Neurosci Dept Florence Italy;
Univ Washington Dept Pediat Seattle WA 98195 USA;
Hosp Miguel Servet Serv Biochem Genet Unit Zaragoza Spain;
CHU Bordeaux Serv Genet Med Bordeaux France;
CHU Bordeaux Lab Genet Mol Bordeaux France;
Boston Childrens Hosp Div Genet &
Genom Boston MA USA;
Univ Groningen Univ Med Ctr Groningen Dept Genet Groningen Netherlands;
Tartu Univ Hosp Dept Clin Genet Tartu Estonia;
Tartu Univ Hosp Dept Clin Genet Tartu Estonia;
Dartmouth Hitchcock Med Ctr Dept Pediat Lebanon NH 03766 USA;
CHRU Lille Inst Genet Med Lille France;
CHRU Strasbourg Hop Civil Lab Diagnost Genet Strasbourg France;
CHRU Strasbourg Hop Civil Lab Diagnost Genet Strasbourg France;
Hop Trousseau Serv Genet &
Embryol Med Paris France;
CHU Paris Ctr Hop Cochin Serv Genet &
Biol Mol Paris France;
Mayo Clin Ctr Individualized Med Rochester MN 55905 USA;
GeneDx Gaithersburg MD USA;
Univ Leuven Ctr Human Genet Leuven Belgium;
CHU Poitiers Lab Genet Serv Genet Poitiers France;
Univ Bourgogne INSERM UMR 1231 GAD Dijon France;
Univ Bourgogne INSERM UMR 1231 GAD Dijon France;
Univ Bourgogne INSERM UMR 1231 GAD Dijon France;
Univ Bourgogne INSERM UMR 1231 GAD Dijon France;
Univ Bourgogne INSERM UMR 1231 GAD Dijon France;
Univ Bourgogne INSERM UMR 1231 GAD Dijon France;
Univ Bourgogne INSERM UMR 1231 GAD Dijon France;
Univ Bourgogne INSERM UMR 1231 GAD Dijon France;
Seattle Childrens Res Inst Ctr Integrat Brain Res Seattle WA USA;
Seattle Childrens Res Inst Ctr Integrat Brain Res Seattle WA USA;
CHU Dijon Bourgogne Hop Enfants Ctr Genet Dijon France;
机译:De Novo TBR1变体导致具有ID和自闭症的神经认知表型:举报25个新个人和文献审查
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机译:De Novo TBR1变体导致具有ID和自闭症的神经认知表型:报告25个新个人和对文献的审查
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