The FMR1 premutation as a cause of premature ovarian failure in Brazilian women
Author:
Affiliation:
1. Universidade de São Paulo, Brazil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v29n3/30743.pdf
Reference41 articles.
1. Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene;Aittomaki K;J Clin Endocr Metab,1996
2. Fragile X premutation is a significant risk factor for premature ovarian failure - The International Collaborative POF in Fragile X Study - Preliminary data;Allingham-Hawkins DJ;Am J Med Genet,1999
3. A novel phenotype related to partial loss of function mutations of the follicle stimulating hormone receptor;Beau I;J Clin Invest,1998
4. A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: Evidence for conserved function in oogenesis and implications for human sterility;Bione S;Am J Hum Genet,1998
5. Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: A pilot study;Braat DD;Am J Med Genet,1999
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1. Molecular Diagnosis of X-Fragile Syndrome: Perspectives for the Public Health System in the Central Region of Brazil;Genetics and Molecular Research;2017
2. Standardization of capillary electrophoresis for diagnosis of fragile X syndrome in the Brazilian public health system;ELECTROPHORESIS;2016-10-19
3. Gene variation and premature ovarian failure: a meta-analysis;European Journal of Obstetrics & Gynecology and Reproductive Biology;2014-11
4. Association between fragile X premutation and premature ovarian failure: a case–control study and meta-analysis;Archives of Gynecology and Obstetrics;2014-01-23
5. The fragile x-associated tremor and ataxia syndrome (FXTAS);Arquivos de Neuro-Psiquiatria;2010-10
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