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See Latest ArticlesCGG repeat sizing in the FMR1 gene in Indian women with premature ovarian failure
Reproductive BioMedicine Online, 09/24/09
Chatterjee S et al. – The results of the study indicate that FMR1 premutations are rare in sporadic cases of POF with no family history of fragile X syndrome. However, although in the normal polymorphic range, expansion of the CGG repeat tract to beyond 30 repeats was associated with serum FSH concentrations in both POF cases and controls.
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