作者：
Beunders, Gea [1]
;
van de Kamp, Jiddeke [2]
;
Vasudevan, Pradeep [3]
;
Morton, Jenny [4]
;
Smets, Katrien [5]
;
Kleefstra, Tjitske [6]
;
de Munnik, Sonja A. [7]
;
Schuurs-Hoeijmakers, Janneke [8]
;
Ceulemans, Berten [9]
;
Zollino, Marcella [10]
;
Hoffjan, Sabine [11]
;
Wieczorek, Stefan [12]
;
So, Joyce [13]
;
Mercer, Leanne ;
Walker, Tanya ;
Velsher, Lea ;
Parker, Michael J. ;
Magee, Alex C. ;
Elffers, Bart ;
Kooy, R. Frank ;
Yntema, Helger G. ;
Meijers-Heijboer, Elizabeth J. ;
Sistermans, Erik A.
作者单位：
Univ & Univ Hosp Antwerp, Dept Med Genet, Antwerp, Belgium
[1]
Univ Cattolica Sacro Cuore, A Gemelli Sch Med, Inst Med Genet, Rome, Italy
[2]
Vrije Univ Amsterdam, Med Ctr Amsterdam, Dept Clin Genet, Recept D,Boellelaan 1117, NL-1081 HV
[3]
Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands
[4]
Northwestern Ontario Reg Genet Program, Thunder Bay Dist Hlth Unit, Thunder Bay, ON, Canada
[5]
Birmingham Womens Hosp, Dept Clin Genet, Birmingham, W Midlands, England
[6]
Belfast City Hosp, Genet Med, Belfast, Antrim, North Ireland
[7]
AMSTA, Dept Med Care Patients Intellectual Disabil, Amsterdam, Netherlands
[8]
Univ Antwerp Hosp, Dept Neurol, Antwerp, Belgium
[9]
Ruhr Univ Bochum, Dept Human Genet, Bochum, Germany
[10]
Sheffield Childrens Hosp, Dept Clin Genet, Sheffield, S Yorkshire, England
[11]
Univ & Univ Hosp Antwerp, Dept Neurol Paediat Neurol, Antwerp, Belgium
[12]
Univ Hosp Leicester, Dept Clin Genet, Leicester, Leics, England
[13]
发布时间
2017-04-06
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