A novel luteinizing hormone/chorionic gonadotropin receptor mutation associated with amenorrhea, low oocyte yield, and recurrent pregnancy loss
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference14 articles.
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2. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene;Kremer;Nat Genet,1995
3. Brief report: testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene;Latronico;N Engl J Med,1996
4. A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia;Laue;Hum Mol Genet,1995
5. Compound heterozygous mutations of the luteinizing hormone receptor gene in Leydig cell hypoplasia;Laue;Mol Endocrinol,1996
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1. A rare cause of primary amenorrhea: LHCGR gene mutations;European Journal of Obstetrics & Gynecology and Reproductive Biology;2022-05
2. Regulation of antral follicular growth by an interplay between gonadotropins and their receptors;Journal of Assisted Reproduction and Genetics;2022-03-15
3. Effects of HRG and TP73 gene variations on ovarian response;Gynecological Endocrinology;2021-09-08
4. Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome;Journal of Assisted Reproduction and Genetics;2020-08-28
5. Genetics of premature ovarian insufficiency;Human Reproductive Genetics;2020
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