R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
about
Central hypogonadotropic hypogonadism: genetic complexity of a complex diseasePrevalence of KISS1 Receptor mutations in a series of 603 patients with normosmic congenital hypogonadotrophic hypogonadism and characterization of novel mutations: a single-centre study.Iron Overload Exacerbates Busulfan-Melphalan Toxicity Through a Pharmacodynamic Interaction in Mice.
P2860
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
@ast
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
@en
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
@nl
type
label
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
@ast
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
@en
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
@nl
prefLabel
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
@ast
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
@en
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
@nl
P2093
P2860
P50
P1433
P1476
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
@en
P2093
Anne Guiochon-Mantel
Frederique Albarel
Jacques Young
Jerome Bouligand
Joelle Cohen-Tannoudji
Luigi Maione
Marc Lombes
Megan Gallant
Philippe Bouchard
P2860
P304
P356
10.1371/JOURNAL.PONE.0069616
P407
P577
2013-07-25T00:00:00Z