作者：
Dias, Cristina [1]
;
Estruch, Sara B. [2]
;
Graham, Sarah A. [3]
;
McRae, Jeremy [4]
;
Sawiak, Stephen J. [5]
;
Hurst, Jane A. [6]
;
Joss, Shelagh K. [7]
;
Holder, Susan E. [8]
;
Morton, Jenny E. V. [9]
;
Turner, Claire [10]
;
Thevenon, Julien [11]
;
Mellul, Kelly [12]
;
Sanchez-Andrade, Gabriela ;
Ibarra-Soria, Ximena ;
Deriziotis, Pelagia ;
Santos, Rui F. ;
Lee, Song-Choon ;
Faivre, Laurence ;
Kleefstra, Tjitske ;
Liu, Pentao ;
Hurles, Mathew E. ;
Fisher, Simon E. ;
Logan, Darren W.
作者单位：
London North West Healthcare NHS Trust, North West Thames Reg Genet Serv, Harrow HA1 3UJ, Middx
[1]
Univ Sorbonne Paris Cite, Hop Necker Enfants Malad, Serv Genet, APHP,Inst Imagine,INSERM,UMR1163, F
[2]
Wellcome Trust Sanger Inst, Wellcome Genome Campus, Hinxton CB10 1SA, England
[3]
Birmingham Womens Hosp, Birmingham Womens NHS Fdn Trust, West Midlands Reg Genet Serv, Birmingham
[4]
Royal Devon & Exeter Hosp Heavitree, Royal Devon & Exeter NHS Fdn Trust, Dept Clin Genet, Peninsula
[5]
Ctr Hosp Univ Dijon, Federat Hosp Univ Med Translat & Anomalies Dev TR, F-21079 Dijon, France
[6]
Great Ormond St Hosp Sick Children, North East Thames Reg Genet Serv, London WC1N 3JH, England
[7]
Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
[8]
Queen Elizabeth Univ Hosp, West Scotland Reg Genet Serv, Level 2 Lab Med Bldg, Glasgow G51 4TF
[9]
Univ Cambridge, Behav & Clin Neurosci Inst, Cambridge CB2 3EB, England
[10]
Max Planck Inst Psycholinguist, Language & Genet Dept, POB 310, NL-6500 AH Nijmegen, Netherlands
[11]
Royal Manchester Childrens Hosp, Childrens Radiol Dept, Manchester M13 9WL, Lancs, England
[12]
发布时间
2017-04-06
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