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See Latest ArticlesGenomic imprinting disorders in humans: a mini-review
Journal of Assisted Reproduction and Genetics, 10/23/09
Butler MG – The first report in humans occurred in Prader–Willi syndrome due to a paternal deletion of chromosome 15 or uniparental disomy 15 (both chromosome 15s from only one parent) and similar genetic disturbances were reported later in Angelman syndrome.
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Sperm chromatin structure is associated with the quality of spermatogenesis in infertile patients
Fertility and Sterility, 12/18/09
B lymphocyte stimulator -817C>T promoter polymorphism and the predisposition for the development of deep infiltrating endometriosis
Fertility and Sterility, 12/18/09
An aromatase polymorphism modulates the relationship between weight and estradiol levels in obese men
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