Male infertility is a major and growing health problem with an estimated global prevalence of 4.2%. The current therapy is limited by the unknown etiology of MI, emphasizing the critical requirement f
We report a rare case of infertility presenting with a 47, XYY mosaicism and congenital bilateral absence of vas deferens. With our patient's informed written consent, we performed a complete set of g
native top-down MS data of human protamines collected on orbitrap fusion lumos. Samples were collected from different patient populations, namely normal, asthenozoospermia, and oliogoasthenozoospermia
Two chromosomal abnormalities are described in an infertile man suffering from teratozoospermia: balanced reciprocal translocation t (17; 22) (p11.2; q11.2) and a microduplication in the region 10q23.