1. P-536 Common variation in the PIN1 locus increases the genetic risk to suffer from Sertoli Cell Only syndrome. (30th June 2022) Authors: Cerván Martín, M; González-Muñoz, S; Bossini-Castillo, L; Guzmán-Jime'nez, A; Garrido, N; Luján, S; Clavero, A; Azoonomic, S.G; Barros, A; Seixas, S; Gonçalves, J; Larriba, S; Lopes, A.M; Carmona, F.D; Palomino-Morales, R.J Journal: Human reproduction Issue: Volume 37(2022)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. P-538 KATNAL1 polymorphisms confer susceptibility to severe phenotypes of male infertility in a large European cohort. (30th June 2022) Authors: GUZMÁN JIMÉNEZ, A; Cerván-Martín, M; Bossini-Castillo, L; Garrido, N; Luján, S; Castilla, J.A; Azoonomic, S.G; Marques, P.I; Carvalho, F; Gonçalves, J; Larriba, S; Lopes, A.M; Palomino-Morales, R.J; Carmona, F.D Journal: Human reproduction Issue: Volume 37(2022)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗