Genetics of primary ovarian insufficiency: new developments and opportunities

Author:

Qin Yingying,Jiao Xue,Simpson Joe Leigh,Chen Zi-Jiang

Funder

National Basic Research Program of China

National Natural Science Foundation of China

Key Program of National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynaecology,Reproductive Medicine

Reference237 articles.

1. Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure;Aboura;J Clin Endocrinol Metab,2009

2. ACOG committee opinion. No. 338: Screening for fragile X syndrome;Obstet Gynecol,2006

3. The genetics of XX gonadal dysgenesis;Aittomäki;Am J Hum Genet,1994

4. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure;Aittomäki;Cell,1995

5. Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene;Aittomäki;J Clin Endocrinol Metab,1996

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