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Evaluating Charge Syndrome in Congenital Hypogonadotropic Hypogonadism Patients Harboring Chd7 Variants

AuthID
P-00P-JR5

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

Pignatelli, D

Niederlander, NJ

Acierno, J

Pitteloud, N

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Document Type

Article

Year published

2018

Published

in GENETICS IN MEDICINE, ISSN: 1098-3600

Volume: 20, Issue: 8, Pages: 872-881 (10)

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Publication Identifiers

DOI: 10.1038/gim.2017.197

Pubmed: 29144511

SCOPUS: 2-s2.0-85045167713

Wos: WOS:000443401600013

Source Identifiers

ISSN: 1098-3600

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All authors

Name Order	Name	Name Order	Name	Name Order	Name
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;

Evaluating Charge Syndrome in Congenital Hypogonadotropic Hypogonadism Patients Harboring Chd7 Variants

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