作者：
Van Esch, Hilde [1]
;
Colnaghi, Rita [2]
;
Freson, Kathleen [3]
;
Starokadomskyy, Petro [4]
;
Zankl, Andreas [5]
;
Backx, Liesbeth [6]
;
Abramowicz, Iga [7]
;
Outwin, Emily [8]
;
Rohena, Luis [9]
;
Faulkner, Claire [10]
;
Leong, Gary M. [11]
;
Newbury-Ecob, Ruth A. [12]
;
Challis, Rachel C. [13]
;
Ounap, Katrin [14]
;
Jaeken, Jacques ;
Seuntjens, Eve ;
Devriendt, Koen ;
Burstein, Ezra ;
Low, Karen J. ;
O'Driscoll, Mark
作者单位：
Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[1]
Katholieke Univ Leuven, Dept Biol, Dev Neurobiol, B-3000 Leuven, Belgium
[2]
Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, Belgium
[3]
Katholieke Univ Leuven, Lab Genet Cognit, Dept Human Genet, B-3000 Leuven, Belgium
[4]
Univ Hosp NHS Trust, St Michaels Hosp, Clin Genet, Bristol BS2 8HW, Avon, England
[5]
Univ Tartu, Tartu Univ Hosp, Dept Clin Genet, United Labs, EE-50406 Tartu, Estonia
[6]
Univ Sussex, Genome Damage & Stabil Ctr, Sussex BN1 9RQ, England
[7]
Southmead Hosp, Bristol Genet Lab, Bristol BS10 5NB, Avon, England
[8]
Univ Sydney, Nepean Clin Sch, Nepean Hosp, Dept Paediat, Kingswood, NSW 2747, Australia
[9]
Univ Edinburgh, MRC Human Genet Unit, Inst Genet & Mol Med, Edinburgh EH4 2XU, Midlothian, Scotland
[10]
Katholieke Univ Leuven, Ctr Mol & Vasc Biol, Dept Cardiovasc Sci, B-3000 Leuven, Belgium
[11]
Childrens Hosp Westmead, Dept Clin Genet, Westmead, NSW 2145, Australia
[12]
San Antonio Mil Med Ctr, Dept Pediat, Div Genet, San Antonio, TX 78234 USA
[13]
Univ Hosp Leuven, Ctr Metab Dis, B-3000 Leuven, Belgium
[14]
发布时间
2020-03-10
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