作者：
Astuti,D. [1]
;
Morris,M.R. [2]
;
Cooper,W.N. [3]
;
Staals,R.H.J. [4]
;
Wake,N.C. [5]
;
Fews,G.A. [6]
;
Gill,H. [7]
;
Gentle,D. ;
Shuib,S. ;
Ricketts,C.J. ;
Cole,T. ;
VanEssen,A.J. ;
VanLingen,R.A. ;
Neri,G. ;
Opitz,J.M. ;
Rump,P. ;
Stolte-Dijkstra,I. ;
Müller,F. ;
Pruijn,G.J.M. ;
Latif,F. ;
Maher,E.R.
作者单位：
Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen
[1]
Istituto di Genetica Medica, Università Cattolica Del Sacro Cuore, Rome, Italy
[2]
Centre for Rare Diseases and Personalised Medicine, School of Clinical and Experimental Medicine
[3]
West Midlands Region Genetics Service, Birmingham Women's Hospital, Edgbaston, Birmingham, United
[4]
Department of Pediatrics, Isala Clinics, Zwolle, Netherlands
[5]
Departments of Pediatrics, Human Genetics, Obstetrics and Gynecology, Salt Lake City, UT, United
[6]
Department of Biomolecular Chemistry, Nijmegen Center for Molecular Life Sciences, Radboud
[7]
发布时间
2013-11-20
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