作者：
Béna,F. [1]
;
Bruno,D.L. [2]
;
Eriksson,M. [3]
;
vanRavenswaaij-Arts,C. [4]
;
Stark,Z. [5]
;
Dijkhuizen,T. [6]
;
Gerkes,E. [7]
;
Gimelli,S. [8]
;
Ganesamoorthy,D. [9]
;
Thuresson,A.C. [10]
;
Labalme,A. [11]
;
Till,M. [12]
;
Bilan,F. [13]
;
UniversitédePoitiers,Poitiers ;
Pasquier,L. ;
Kitzis,A. ;
Dubourgm,C. ;
Rossi,M. ;
Bottani,A. ;
Gagnebin,M. ;
Sanlaville,D. ;
Gilbert-Dussardier,B. ;
Guipponi,M. ;
vanHaeringen,A. ;
Kriek,M. ;
Ruivenkamp,C. ;
Antonarakis,S.E. ;
Anderlid,B.M. ;
Slater,H.R. ;
Schoumans,J.
作者单位：
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Parkville, VIC
[1]
Service of Genetic Medicine, Geneva University Hospital, Geneva, Switzerland, Department of Genetic
[2]
Service de Génétique Médicale-H?pital Sud-CHU Rennes, Rennes, France
[3]
Center for Human and Clinical Genetics, Leiden University Medical Center (LUMC), Leiden, Netherlands
[4]
Department of Genetics, University of Groningen, University Medical Center Groningen (UMCG),
[5]
Service de Génétique, Centre Hospitalier Universitaire de Poitiers, France
[6]
Department of Neuropediatrics, Astrid Lindgren Children's Hospital, Stockholm, Sweden, Department
[7]
Department of Immunology, Genetics and Pathology, The Rudbeck Laboratory, Uppsala University
[8]
Department of Womeńs and Childreńs Health, Karolinska Institutet, Stockholm, Sweden
[9]
Service de Cytogénétique Constitutionnelle, Hospices Civils de Lyon, Groupement Hospitalier Est
[10]
Department of Molecular Medicine and Surgery, CMM, Karolinska Institutet, Stockholm, Sweden
[11]
Service of Genetic Medicine, Geneva University Hospital, Geneva, Switzerland
[12]
Poitiers, France
[13]
发布时间
2013-11-20
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