Familial Premature Ovarian Failure in Female Premutated Carriers of Fragile X Syndrome: a Case Report and Literature Review-Reference-Cited by-同舟云学术

Familial Premature Ovarian Failure in Female Premutated Carriers of Fragile X Syndrome: a Case Report and Literature Review

Published:2006-03 Issue:1 Volume:45 Page:60-63
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Lin Yu-Shiou,Yang Man-Li

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference19 articles.

1. The Metabolic and Molecular Basis of Inherited Diseases;Scriver,2002

2. Prevalence of carriers of premutation-size alleles of the FMR1 gene and implications for the population genetics of the fragile X syndrome;Rousseau;Am J Med Genet,1995

3. Prevalence of fragile X syndrome;Turner;Am J Med Genet,1996

4. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome;Oberle;Science,1991

5. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence P(CGG)n;Kremer;Science,1991

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2. Association between premature ovarian failure, polymorphisms in MTHFR and MTRR genes and serum homocysteine concentration;Reproductive BioMedicine Online;2016-04

3. Genetics of premature ovarian failure;Current Opinion in Obstetrics & Gynecology;2015-06

4. Unstable Mutations in the FMR1 Gene and the Phenotypes;Advances in Experimental Medicine and Biology;2012

5. Genetic aspects of premature ovarian failure: a literature review;Archives of Gynecology and Obstetrics;2010-12-29