作者:
Michot,C. [1]
;
LeGoff,C. [2]
;
Mahaut,C. [3]
;
Afenjar,A. [4]
;
Brooks,A.S. [5]
;
Campeau,P.M. [6]
;
Destree,A. [7]
;
DiRocco,M. [8]
;
Donnai,D. [9]
;
Hennekam,R. [10]
;
Heron,D. [11]
;
Jacquemont,S. [12]
;
Kannu,P. [13]
;
Lin,A.E. [14]
;
Manouvrier-Hanu,S. [15]
;
Mansour,S. [16]
;
Marlin,S. [17]
;
McGowan,R. [18]
;
Murphy,H. [19]
;
Raas-Rothschild,A. [20]
;
Rio,M. [21]
;
Simon,M. [22]
;
Stolte-Dijkstra,I. [23]
;
Stone,J.R. ;
Sznajer,Y. ;
Tolmie,J. ;
Touraine,R. ;
VanDenEnde,J. ;
VanDerAa,N. ;
VanEssen,T. ;
Verloes,A. ;
Munnich,A. ;
Cormier-Daire,V.
作者单位:
Department of Medical Genetics, University and University Hospital AntwerpEdegem, Belgium
[1]
Manchester Academic Health Science Centre, Genetic Medicine-University of Manchester, St Mary's
[2]
Department of Genetics, Paris Descartes University-Sorbonne Paris Cité, Necker Enfants-Malades
[3]
Department of Pathology, Massachussets General HospitalBoston, MA, United States
[4]
Medical Genetics, Massachussets General Hospital for ChildrenBoston, MA, United States
[5]
Genetic and Medical Embryology Unit, Centre de Référence des Surdités Génétiques, Armand-Trousseau
[6]
Department of Clinical Genetics, University HospitalLille, France
[7]
Department of Pediatrics, Academic Medical Center, University of AmsterdamAmsterdam, Netherlands
[8]
Department of Human Genetics, Institute of Pathology and GeneticsGosselies, Belgium
[9]
Department of Genetics, University Medical Center Groningen, University of GroningenGroningen
[10]
Center for Human Genetics, Cliniques Universitaires St-LucBrussels, Belgium
[11]
Division of Clinical and Metabolic Genetics, Hospital for Sick ChildrenToronto, ON, Canada
[12]
Department of Genetics, CHUVVaud, Switzerland
[13]
Neuropediatry Department, Centre de Référence Maladies Rares 'Anomalies du Développement, Armand
[14]
Department of Molecular and Human Genetics, Baylor College of MedicineHouston, TX, United States
[15]
West of Scotland Regional Genetics ServiceGlasgow, United Kingdom
[16]
Department of Clinical Genetics, Ersamus MCRotterdam, Netherlands
[17]
Clinical Genetics, St George's Healthcare NHS TrustLondon, United Kingdom
[18]
Department of Clinical Genetics, Saint-Etienne CHUSaint-Etienne, France
[19]
Institute of Human Genetics, Meir Medical CenterKfar Saba, Israel
[20]
Unit of Rare Diseases, Department of Pediatrics, Gaslini InstituteGenoa, Italy
[21]
Genetics and Cytogenetics Department, GRC-upmc, Pitié-Salpétrière CHUParis, France
[22]
Department of Genetics, INSERM U676, Robert Debré HospitalParis, France
[23]
发布时间
2020-02-26