作者：
Gardeitchik,T. [1]
;
Mohamed,M. [2]
;
Fischer,B. [3]
;
Lammens,M. [4]
;
Lefeber,D. [5]
;
Lace,B. [6]
;
Parker,M. [7]
;
Kim,K.-J. [8]
;
Lim,B.C. [9]
;
H?berle,J. [10]
;
Garavelli,L. [11]
;
Jagadeesh,S. [12]
;
Kariminejad,A. [13]
;
Guerra,D. ;
Le?o,M. ;
Keski-Filppula,R. ;
Brunner,H. ;
Nijtmans,L. ;
VanDenHeuvel,B. ;
Wevers,R. ;
Kornak,U. ;
Morava,E.
作者单位：
Kariminejad-Najmabadi Pathology and Genetics Center, Teheran, Iran
[1]
Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, United Kingdom
[2]
Department of Pediatrics, Seoul National University Hospital, Seoul, South Korea
[3]
Department of Clinical Genetics, Oulu University Hospital, Oulu, Finland
[4]
Clinical Genetics Unit, Obstetric and Pediatric Department, Santa Maria Nuova Hospital IRCCS
[5]
Medical Genetics Clinic, Children's Clinical University Hospital, Riga, Latvia
[6]
Department of Pediatrics, University Children's Hospital, Zürich, Switzerland
[7]
Department of Biomedical Sciences, University of Modena and Reggio Emilia, Modena, Italy
[8]
Pediatric Neurology Unit and Neurogenetics Unit, Hospital S Jo?o, Porto, Portugal
[9]
Institute of Medical Genetics and Human Genetics, Charité Universit?tsmedizin, Berlin, Germany, FG
[10]
Department of Pediatrics, Institute for Metabolic and Genetic Disease, Radboud University Medical
[11]
Institute of Medical Genetics and Human Genetics, Charité Universit?tsmedizin, Berlin, Germany
[12]
Department of Clinical Genetics, Chennai, India
[13]
发布时间
2014-10-16
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