机译:Meis2的杂合态损失变异导致三合会的腭缺损,先天性心脏缺陷和智力残疾
Katholieke Univ Leuven Ctr Human Genet Leuven Belgium;
Maimonides Hosp Infants &
Childrens Hosp Brooklyn Div Med Genet Brooklyn NY USA;
CHU Nantes Serv Genet Med Nantes France;
Univ Med Ctr Utrecht Dept Med Genet Utrecht Netherlands;
Childrens Univ Hosp Dept Clin Genet Temple St Dublin Ireland;
Oxford Univ Hosp NHS Fdn Trust Oxford Ctr Genom Med Oxford England;
Univ Med Ctr Hamburg Eppendorf Inst Human Genet Hamburg Germany;
Icahn Sch Med Mt Sinai Mindich Child Hlth &
Dev Inst New York NY 10029 USA;
CHU Lille Hop Jeanne Flandre Serv Genet Clin Lille France;
Univ Montreal CHU St Justine Dept Pediat Serv Genet Med Montreal PQ Canada;
Manchester Univ Hosp NHS Fdn Trust Manchester Acad Hlth Sci Ctr Manchester Ctr Genom Med;
CHU Pontchaillou Genet Mol Lab Rennes France;
Bambino Gesu Pediat Hosp IRCCS Med Genet Lab Rome Italy;
Rigshosp Appl Human Mol Genet Kennedy Ctr Dept Clin Genet Copenhagen Univ Hosp Glostrup Denmark;
Univ Exeter Sch Med Inst Biomed &
Clin Sci Exeter Devon England;
CHU Nantes Serv Genet Med Nantes France;
McGill Univ Dept Pediat Fac Med Montreal PQ Canada;
Katholieke Univ Leuven Ctr Human Genet Leuven Belgium;
Columbia Univ Dept Pediat Med Ctr Div Clin Genet New York NY 10027 USA;
SG Moscati Hosp Div Med Genet Avellino Italy;
Manchester Univ Hosp NHS Fdn Trust Manchester Acad Hlth Sci Ctr Manchester Ctr Genom Med;
CHU Nantes Serv Genet Med Nantes France;
CHU Nantes Serv Stomatol Nantes France;
Katholieke Univ Leuven Ctr Human Genet Leuven Belgium;
Katholieke Univ Leuven Ctr Human Genet Leuven Belgium;
Rigshosp Appl Human Mol Genet Kennedy Ctr Dept Clin Genet Copenhagen Univ Hosp Glostrup Denmark;
CHU Rennes Serv Genet Med Ctr Reference Anomalies Dev Rennes France;
UZ Leuven Pediat &
Congenital Cardiol Leuven Belgium;
Childrens Hosp Philadelphia Div Cardiol 34th St &
Civic Ctr Blvd Philadelphia PA 19104 USA;
Univ Hosp Leuven Dept Otorhinolaryngol Head &
Neck Surg Leuven Belgium;
Univ Montreal CHU St Justine Dept Pediat Serv Genet Med Montreal PQ Canada;
CHU Rennes Serv Genet Med Ctr Reference Anomalies Dev Rennes France;
Oxford Univ Hosp NHS Fdn Trust Oxford Ctr Genom Med Oxford England;
Univ Med Ctr Hamburg Eppendorf Inst Human Genet Hamburg Germany;
CHU Nantes Serv Genet Med Nantes France;
Bambino Gesu Pediat Hosp IRCCS Med Genet Lab Rome Italy;
CHU Rennes Serv Genet Med Ctr Reference Anomalies Dev Rennes France;
CHU Lille Hop Jeanne Flandre Serv Genet Clin Lille France;
Columbia Univ Med Ctr Inst Genom Med New York NY USA;
Columbia Univ Med Ctr Inst Genom Med New York NY USA;
Helmholtz Zentrum Munchen Inst Human Genet Neuherberg Germany;
Univ Med Ctr Utrecht Dept Med Genet Utrecht Netherlands;
Katholieke Univ Leuven Ctr Human Genet Leuven Belgium;
Katholieke Univ Leuven Ctr Human Genet Leuven Belgium;
机译:Meis2的杂合态损失变异导致三合会的腭缺损,先天性心脏缺陷和智力残疾
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