https://www.selleckchem.com/CDK.html
ith one another. There was a statistically significant but clinically irrelevant difference in the rate of mature oocytes across different variant combinations. Our findings suggest that the presence of gonadotropin receptor polymorphisms in both FSHR N680S and LHCGR N312S are not associated with assisted reproductive technology outcomes; therefore, these variants should not be considered reproductive predictors. Our findings suggest that the presence of gonadotropin receptor polymorphisms in both FSHR N680S and LHCGR N312S are not associated with a
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