Evaluating Charge Syndrome in Congenital Hypogonadotropic Hypogonadism Patients Harboring Chd7 Variants

AuthID
 P-00P-JR5
21
Author(s)
Xu, C
·
Cassatella, D
·
van der Sloot, AM
·
Quinton, R
·
Hauschild, M
·
De Geyter, C
·
Fluck, C
·
Feller, K
·
Bartholdi, D
·
Nemeth, A
·
[+1]·
Djurdjevic, SP
·
Maeder, P
·
Papadakis, G
·
Dwyer, AA
·
Marino, L
·
Favre, L
·
Niederlander, NJ
·
Acierno, J
·
Pitteloud, N
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Tipo de Documento
Article
Year published
2018
Publicado
in GENETICS IN MEDICINE, ISSN: 1098-3600
Volume: 20, Número: 8, Páginas: 872-881 (10)
Indexing
Wos®
Scopus®
Crossref®32
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 29144511
SCOPUS: 2-s2.0-85045167713
Wos: WOS:000443401600013
Source Identifiers
ISSN: 1098-3600
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All authors
Name Order Nome   Name Order Nome   Name Order Nome
1 Xu, C;   2 Cassatella, D;   3 van der Sloot, AM;
4 Quinton, R;   5 Hauschild, M;   6 De Geyter, C;
7 Fluck, C;   8 Feller, K;   9 Bartholdi, D;
10 Nemeth, A;   11 Halperin, I;   12 Djurdjevic, SP;
13 Maeder, P;   14 Papadakis, G;   15 Dwyer, AA;
16 Marino, L;   17 Favre, L;   18 Pignatelli, D;
19 Niederlander, NJ;   20 Acierno, J;   21 Pitteloud, N;

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