Array Comparative Genomic Hybridization Profiling Analysis Reveals Deoxyribonucleic Acid Copy Number Variations Associated with Premature Ovarian Failure

Author:

Aboura Azzedine1,Dupas Claire2,Tachdjian Gérard3,Portnoï Marie-France4,Bourcigaux Nathalie2,Dewailly Didier5,Frydman René6,Fauser Bart7,Ronci-Chaix Nathalie8,Donadille Bruno2,Bouchard Philippe2,Christin-Maitre Sophie2

Affiliation:

1. Department of Cytogenetics (A.A.), Robert Debré Hospital, 75019 Paris, France

2. Department of Endocrinology (C.D., N.B., B.D., P.B., S.C.-M.), Saint-Antoine Hospital, Centre de Référence des Maladies, Endocriniennes Rares de la Croissance, Assistance Publique-Hôpitaux de Paris, ER9 University Pierre et Marie Curie, 75005 Paris, France

3. Department of Embryology and Cytogenetics (G.T.), Institut National de la Santé et de la Recherche Médicale (INSERM) Unité 935, 92140 Clamart, France

4. Department of Genetics and Embryology (M.-F.P.), Armand Trousseau Hospital, 75012 Paris, France

5. Department of Reproductive Endocrinology (D.D.), Jeanne de Flandre Hospital, 59000 Lille, France

6. Department of Obstetrics and Gynecology (R.F.), Antoine Béclère Hospital, INSERM U782, University Paris 11, 92140 Clamart, France

7. Department of Reproductive Medicine and Gynecology (B.F.), University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands

8. Department of Endocrinology (N.R.-C.), Haut Lévèque Hospital, 33604 Bordeaux, France

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference41 articles.

1. Premature ovarian failure.;Goswami;Hum Reprod Update,2005

2. Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers.;Ennis;Eur J Hum Genet,2006

3. Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure.;Di Pasquale;J Clin Endocrinol Metab,2006

4. Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.;Laissue;Eur J Endocrinol,2006

5. A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics.;Allen;Hum Reprod,2003

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