Premature ovarian failure and androgen receptor gene CAG repeat lengths weighted by X chromosome inactivation patterns
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology,Reproductive Medicine
Reference20 articles.
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2. Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene;Di Pasquale;Am J Hum Genet,2004
3. Identification of novel mutations in FOXL2 associated with premature ovarian failure;Harris;Mol Hum Reprod,2002
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1. Investigation of the role of X chromosome inactivation and androgen receptor CAG repeat polymorphisms in patients with recurrent pregnancy loss: a prospective case–control study;BMC Pregnancy and Childbirth;2022-11-02
2. The Genetics of Non-Syndromic Primary Ovarian Insufficiency: A Systematic Review;INT J FERTIL STERIL;2019
3. Microsatellite variation of ESR1, ESR2, and AR in Serbian women with primary ovarian insufficiency;Climacteric;2018-08-29
4. A pharmacogenetic approach to improve low ovarian response: The role of CAG repeats length in the androgen receptor gene;European Journal of Obstetrics & Gynecology and Reproductive Biology;2018-08
5. Triacylglyceride physiology in the short-finned eel, Anguilla australis—the effects of androgen;American Journal of Physiology-Regulatory, Integrative and Comparative Physiology;2016-03-01
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