No Evidence for Parent of Origin Influencing Premature Ovarian Failure in Fragile X Premutation Carriers
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference4 articles.
1. Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations;Hundscheid;Am J Hum Genet,2000
2. Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus;Morton;Proc Natl Acad Sci USA,1992
3. Murray A, Ennis S, MacSwiney F, Webb J, Morton N. Reproductive and menstrual history of females with fragile X expansions. Eur J Hum Genet (in press)
4. Studies of FRAXA and FRAXE in women with premature ovarian failure;Murray;J Med Genet,1998
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2. Laboratory testing for fragile X, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG);Genetics in Medicine;2021-05
3. Fragile X-Associated Diminished Ovarian Reserve and Primary Ovarian Insufficiency from Molecular Mechanisms to Clinical Manifestations;Frontiers in Molecular Neuroscience;2017-09-12
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5. Early menopause: A hazard to a woman's health;Indian Journal of Medical Research;2016
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