作者：
Michot, Caroline [1]
;
Le Goff, Carine [2]
;
Blair, Edward [3]
;
Blanchet, Patricia [4]
;
Capri, Yline [5]
;
Gilbert-Dussardier, Brigitte [6]
;
Goldenberg, Alice [7]
;
Henderson, Alex [8]
;
Isidor, Bertrand [9]
;
Kayserili, Hulya [10]
;
Kinning, Esther [11]
;
Le Merrer, Martine [12]
;
Lyonnet, Stanislas [13]
;
Odent, Sylvie [14]
;
Simsek-Kiper, Pelin Ozlem [15]
;
Quelin, Chloe ;
Savarirayan, Ravi ;
Simon, Marleen ;
Splitt, Miranda ;
Verhagen, Judith M. A. ;
Verloese, Alain ;
Munnich, Arnold ;
Baujat, Genevieve ;
Cormier-Daire, Valerie
作者单位：
Paris Descartes Sorbonne Paris Cite Univ, Necker Enfants Malad Hosp, IMAGINE Inst, Dept Med Genet
[1]
Inst Genet Med, Northern Genet Serv, Newcastle Upon Tyne, Tyne & Wear, England
[2]
Robert Debre Hosp, Dept Med Genet, INSERM U676, Paris, France
[3]
Murdoch Childrens Res Inst, Victorian Clin Genet Serv, Melbourne, Vic, Australia
[4]
Hacettepe Univ, Dept Pediat, Pediat Genet Unit, Fac Med, Ankara, Turkey
[5]
CHU Rouen, Dept Genet, Ctr Med Genom & Personalized Med Normandy, Rouen, France
[6]
Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands
[7]
Oxford Univ Hosp NHS Fdn Trust Headington, Nuffield Orthopaed Ctr, Oxford Ctr Genom Med, ACE Bldg
[8]
CHRU Montpellier, Arnaud de Villeneuve Hosp, Dept Med Genet, Montpellier, France
[9]
Royal Hosp Sick Children, Ferguson Smith Ctr Clin Genet, Glasgow, Lanark, Scotland
[10]
Erasmus Univ, Dept Clin Genet, Med Ctr, Rotterdam, Netherlands
[11]
Istanbul Univ, Istanbul Fac Med, Dept Med Genet, Istanbul, Turkey
[12]
CHU La Miletrie, Dept Genet, Poitiers, France
[13]
Rennes Univ, CHU Rennes, Dept Clin Genet, CNRS IGDR,Inst Genet & Dev Rennes,UMR6290, Rennes, France
[14]
CHU Nantes, Dept Med Genet, Nantes, France
[15]
发布时间
2020-05-12
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