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Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report
BACKGROUND: The association between premature ovarian failure (POF) and the FMR1 repeat number (41> CGG(n)< 200) has been widely investigated. Current findings suggest that the risk estimation for POF can be calculated in the offspring of women with pre-mutated FMR1 alleles. CASE PRESENTATION:...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2007
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1859987/ https://ncbi.nlm.nih.gov/pubmed/17428316 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-8-18 |
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