作者：
Brian,Sperelakis-Beedham [1]
;
Agnès,Taillandier [1]
;
Christelle,Domingues [1]
;
Mihelaiti,Guberto [1]
;
Estelle,Colin [2]
;
Valérie,Porquet-Bordes [3]
;
Anya,Rothenbuhler [4]
;
Jean-Pierre,Salles [3]
;
Deborah,Wenkert [5]
;
Andreas,Zankl [6]
;
Christine,Muti [1]
;
Séverine,Bacrot [1]
;
Brigitte,Simon-Bouy [1]
;
Etienne,Mornet [7]
作者单位：
Unité de Génétique constitutionnelle, Centre Hospitalier de Versailles, Le Chesnay, France.
[1]
Service de Génétique Médicale, CHU, Angers, France.
[2]
Pédiatrie - Endocrinologie, génétique et gynécologie médicale, Hôpital des enfants (CHU Toulouse), Toulouse, France.
[3]
Service d'endocrinologie et diabète de l'enfant, Hôpital Bicêtre (Hôpitaux Universitaires Paris Saclay - APHP), Paris, France.
[4]
Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children - St. Louis, St. Louis, MO 63110, USA; Wenkert & Young, LLC, Thousand Oaks, CA 91362, USA.
[5]
Department of Clinical Genetics, Sydney Children's Hospital Network (Westmead), Westmead, Australia; Faculty of Medicine and Health, The University of Sydney, Sydney, Australia; Bone Biology Division and Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, Australia.
[6]
Unité de Génétique constitutionnelle, Centre Hospitalier de Versailles, Le Chesnay, France. Electronic address: emornet@ch-versailles.fr.
[7]
DOI
10.1016/j.ymgme.2021.01.009
PMID
33549410
发布时间
2021-08-05
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