作者：
Aitken, Stuart [1]
;
Firth, Helen V. [2]
;
McRae, Jeremy [3]
;
Halachev, Mihail [4]
;
Kini, Usha [5]
;
Parker, Michael J. [6]
;
Lees, Melissa M. [7]
;
Lachlan, Katherine [8]
;
Sarkar, Ajoy [9]
;
Joss, Shelagh [10]
;
Splitt, Miranda [11]
;
McKee, Shane [12]
;
Nemeth, Andrea H. ;
Scott, Richard H. ;
Wright, Caroline F. ;
Marsh, Joseph A. ;
Hurles, Matthew E. ;
FitzPatrick, David R. ;
DDD Study
作者单位：
Northern Genet Serv,Newcastle Upon Tyne Hosp NHS Fdn Trust
[1]
Wellcome Sanger Inst
[2]
MRC Human Genet Unit,Univ Edinburgh
[3]
Sch Med,Univ Exeter
[4]
Oxford Ctr Genom Med,Oxford Univ Hosp NHS Fdn Trust
[5]
Sheffield Childrens Hosp NHS Fdn Trust
[6]
North East Thames Reg Genet Serv,Great Ormond St Hosp Children NHS Fdn Trust
[7]
Wessex Clin Genet Serv,Univ Hosp Southampton NHS Trust
[8]
Nottingham Reg Genet Serv City,Nottingham Univ Hosp NHS Trust
[9]
West Scotland Reg Genet Serv,Queen Elizabeth Univ Hosp
[10]
Northern Ireland Reg Genet Serv,Belfast City Hosp
[11]
Nuffield Dept Clin Neurosci,Univ Oxford
[12]
发布时间
2022-10-29
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