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You searched for: Author/Creator Seixas, S

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2. O-118 New insight into the genetic contribution of common variants to the development of extreme phenotypes of unexplained male infertility: a multicenter genome-wide association study. (6th August 2021)

3. P-536 Common variation in the PIN1 locus increases the genetic risk to suffer from Sertoli Cell Only syndrome. (30th June 2022)