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Screening for FOXL2 gene mutations in women with premature ovarian failure: an Indian experience

  • Published:2007-01 Issue:5 Volume:15 Page:554-560
  • ISSN:1472-6483
  • Container-title:Reproductive BioMedicine Online
  • language:en
  • Short-container-title:Reproductive BioMedicine Online

Author:

Chatterjee Suparna,Modi Deepak,Maitra Anurupa,Kadam Seema,Patel Zarine,Gokral Jyotsna,Meherji Pervin

Publisher

Elsevier BV

Subject

Developmental Biology,Reproductive Medicine,Obstetrics and Gynaecology

Reference28 articles.

1. Premature ovarian failure: an update;Anasti;Fertility and Sterility,1998

2. X chromosome genes and premature ovarian failure;Bione;Seminars in Reproductive Medicine,2000

3. Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure;Bodega;Molecular Human Reproduction,2004

4. Evolution and expression of FOXL2;Cocquet;Journal of Medical Genetics,2002

5. Premature ovarian failure;Conway;Current Opinion in Obstetrics and Gynecology,1997

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