机译:FBXW11中的De Novo Missense Variants导致不同的发育表型,包括大脑,眼睛和数字异常
Oxford Brookes Univ Fac Hlth &
Life Sci Oxford OX3 0BP England;
UCL Dept Cell &
Dev Biol Gower St London WC1E 6BT England;
UCL Great Ormond St Inst Child Hlth London WC1N 1EH England;
Oxford Brookes Univ Fac Hlth &
Life Sci Oxford OX3 0BP England;
Univ Calif San Francisco Fresno Genet Med Fresno CA 93701 USA;
Osped Pediat Bambino Gesu Genet &
Rare Dis Res Div Sci Inst Res Hosp &
Healthcare I-00146 Rome;
Oxford Brookes Univ Fac Hlth &
Life Sci Oxford OX3 0BP England;
Osped Pediat Bambino Gesu Genet &
Rare Dis Res Div Sci Inst Res Hosp &
Healthcare I-00146 Rome;
Univ Med Ctr Utrecht Dept Genet NL-3508 GA Utrecht Netherlands;
Odense Univ Hosp Dept Clin Genet DK-5000 Odense C Denmark;
Univ Med Ctr Utrecht Dept Genet NL-3508 GA Utrecht Netherlands;
Fdn Casa Sollievo della Sofferenza Mol Genet Unit I-71013 San Giovanni Rotondo Italy;
Osped San Martino Unita Operat Complessa Pediat &
Patol Neonatale I-32100 Belluno Italy;
Univ Washington Seattle WA 98195 USA;
Birmingham Womens &
Childrens Natl Hlth Serv Fdn West Midlands Reg Genet Lab Mindelsohn Way;
Birmingham Womens &
Childrens Natl Hlth Serv Fdn West Midlands Reg Genet Lab Mindelsohn Way;
Univ Toulouse UDEAR Inst Natl Sante &
Rech Med UMRS 1056 Univ Paul Sabatier F-31059 Toulouse;
Duke Univ Sch Med Program Genet &
Genom Dept Pediat &
Neurobiol Durham NC 27710 USA;
Odense Univ Hosp Dept Clin Genet DK-5000 Odense C Denmark;
Odense Univ Hosp Hans Christian Andersen Childrens Hosp DK-5000 Odense C Denmark;
Duke Univ Med Ctr Div Med Genet Dept Pediat Durham NC 27710 USA;
Ambry Genet Dept Clin Affairs Aliso Viejo CA 92656 USA;
Kennedy Krieger Inst Div Neurogenet Dept Neurol Baltimore MD 21205 USA;
Kennedy Krieger Inst Div Neurogenet Dept Neurol Baltimore MD 21205 USA;
AstraZeneca Ctr Genom Res Discovery Sci Biopharmaceut R&
D Cambridge CB4 0WG England;
Birmingham Womens &
Childrens Natl Hlth Serv Fdn West Midlands Reg Genet Lab Mindelsohn Way;
Duke Univ Med Ctr Div Med Genet Dept Pediat Durham NC 27710 USA;
Icahn Sch Med Mt Sinai Dept Pediat Mindich Child Hlth &
Dev Inst New York NY 10029 USA;
UCL Dept Cell &
Dev Biol Gower St London WC1E 6BT England;
UCL Great Ormond St Inst Child Hlth London WC1N 1EH England;
Osped Pediat Bambino Gesu Genet &
Rare Dis Res Div Sci Inst Res Hosp &
Healthcare I-00146 Rome;
Univ Toulouse UDEAR Inst Natl Sante &
Rech Med UMRS 1056 Univ Paul Sabatier F-31059 Toulouse;
Univ Toulouse UDEAR Inst Natl Sante &
Rech Med UMRS 1056 Univ Paul Sabatier F-31059 Toulouse;
Oxford Brookes Univ Fac Hlth &
Life Sci Oxford OX3 0BP England;
机译:FBXW11中的De Novo Missense Variants导致不同的发育表型,包括大脑,眼睛和数字异常
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机译:神经发育障碍中的Novo畸形突变
机译:FBXW11中的De Novo Missense变异会导致多种发育表型包括脑眼和数字异常
机译:FBXW11中的De Novo Missense Valiants导致不同的发育表型,包括大脑,眼睛和数字异常