Article (Scientific journals)
GPR101 mutations are not a frequent cause of congenital isolated growth hormone deficiency
Castinetti, F; Daly, Adrian; Stratakis, CA et al.
2016In Hormone and Metabolic Research, p. 1-5
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Disciplines :
Endocrinology, metabolism & nutrition
Author, co-author :
Castinetti, F 
Daly, Adrian   ;  Université de Liège > Département des sciences cliniques > Endocrinologie
Stratakis, CA
CABERG, Jean-Hubert ;  Centre Hospitalier Universitaire de Liège - CHU > Génétique
CASTERMANS, Emilie ;  Centre Hospitalier Universitaire de Liège - CHU > Génétique
Trivellin, G
Rostomyan, Liliya  ;  Université de Liège - ULiège > Doct. sc. médicales (Bologne)
Saveanu, A
Jullien, N
Reynaud, R
Barlier, A
Bours, Vincent ;  Université de Liège > Département des sciences biomédicales et précliniques > GIGA-R : Génétique humaine
Brue, T
Beckers, Albert ;  Université de Liège > Département des sciences cliniques > Endocrinologie
More authors (4 more) Less
 These authors have contributed equally to this work.
Language :
English
Title :
GPR101 mutations are not a frequent cause of congenital isolated growth hormone deficiency
Publication date :
2016
Journal title :
Hormone and Metabolic Research
ISSN :
0018-5043
eISSN :
1439-4286
Publisher :
Georg Thieme Verlag Stuttgart, Stuttgart, Germany
Pages :
1-5
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 03 February 2016

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