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Premature menopause in a multi-ethnic population study of the menopause transition, Human Reproduction, vol.18, issue.1, pp.199-206, 2003. ,
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Care of Girls and Women with Turner Syndrome: A Guideline of the Turner Syndrome Study Group, The Journal of Clinical Endocrinology & Metabolism, vol.92, issue.1, pp.10-25, 2007. ,
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Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders, Fertility and Sterility, vol.80, issue.4, pp.1052-1056, 2003. ,
DOI : 10.1016/S0015-0282(03)01121-X
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Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases, Human Reproduction, vol.31, issue.8, pp.1913-1938, 2016. ,
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Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure, Fertility and Sterility, vol.95, issue.5, pp.1595-600, 2011. ,
DOI : 10.1016/j.fertnstert.2010.12.052
Association between idiopathic premature ovarian failure and fragile X premutation, Human Reproduction, vol.15, issue.1, pp.197-202, 2000. ,
DOI : 10.1093/humrep/15.1.197
Premature ovarian failure and fragile X premutation: a study on 45 women, European Journal of Obstetrics & Gynecology and Reproductive Biology, vol.112, issue.2, pp.189-91, 2004. ,
DOI : 10.1016/j.ejogrb.2003.06.003
Premature ovarian failure in the fragile X syndrome, American Journal of Medical Genetics, vol.67, issue.3, pp.189-94, 2000. ,
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EMQN best practice guidelines for the molecular genetic testing and reporting of fragile X syndrome and other fragile X-associated disorders, European Journal of Human Genetics, vol.4, issue.4, pp.417-442, 2015. ,
DOI : 10.1136/jmg.30.5.410
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Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles, American Journal of Medical Genetics Part A, vol.252, issue.4, pp.771-779, 2013. ,
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Elevated Prevalence of 35-44 FMR1 Trinucleotide Repeats in Women With Diminished Ovarian Reserve, Reproductive Sciences, vol.20, issue.6, pp.1226-1257, 2012. ,
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FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure, Human Genetics, vol.12, issue.4, pp.376-82, 2005. ,
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Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure, European Journal of Endocrinology, vol.154, issue.5, pp.739-783, 2006. ,
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Gene in a Large Cohort of Women with Premature Ovarian Failure, The Journal of Clinical Endocrinology & Metabolism, vol.91, issue.5, pp.1976-1985, 2006. ,
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Identification of the forkhead transcriptional factor 2 (FOXL2) gene mutations in four Chinese families with blepharophimosis syndrome, Mol Vis, vol.19, pp.2298-305, 2013. ,