NOBOXis a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency-Reference-Cited by-同舟云学术

NOBOXis a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency

Published:2016-03-04 Issue:5 Volume:89 Page:608-613
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Bouali N.¹,Francou B.²³,Bouligand J.²³,Lakhal B.¹,Malek I.¹,Kammoun M.¹,Warszawski J.⁴,Mougou S.¹,Saad A.¹,Guiochon-Mantel A.²³

Affiliation:

1. Laboratory of Human Cytogenetics, Molecular Genetics and Reproductive Biology; Farhat Hached University Hospital; Sousse 4000 Tunisia

2. Faculté de Médecine Paris Sud; INSERM UMR_S1185, University Paris Saclay, Univ Paris sud; Le Kremlin-Bicêtre France

3. Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, Service de Génétique moléculaire; Pharmacogénétique et Hormonologie; Le Kremlin-Bicêtre France

4. Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, Service d'Epidémiologie; University Paris Saclay, University Paris-Sud, INSERM U1018 eq 4; Le Kremlin-Bicêtre France

Funder

Ministère de l'Enseignement Supérieur et de la Recherche Scientifique

Farhat Hached University Hospital

Assistance Publique - Hôpitaux de Paris

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference19 articles.

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2. Genes involved in human premature ovarian failure;Persani;J Mol Endocrinol,2010

3. Genetic and phenotypic heterogeneity in ovarian failure overview of selected candidate genes;Simpson;Ann NY Acad Sci,2008