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Frontiers in Cell and Developmental Biology|May 31, 2021
TRIM71 Deficiency Causes Germ Cell Loss During Mouse Embryogenesis and Is Associated With Human Male InfertilityLucia A Torres-Fernández, Jana Emich, Yasmine Port, et al.Life Science Alliance|November 29, 2022
Transcriptome analyses in infertile men reveal germ cell-specific expression and splicing patternsLara M Siebert-Kuss, Henrike Krenz, Tobias Tekath, et al.European Urology|June 11, 2022
Genetic Architecture of Azoospermia-Time to Advance the Standard of CareMargot J Wyrwoll, Nils Köckerling, Matthias Vockel, et al.American Journal of Human Genetics|October 22, 2019
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body AsymmetryJulia Wallmeier, Diana Frank, Amelia Shoemark, et al.American Journal of Human Genetics|July 17, 2020
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male InfertilityMargot J Wyrwoll, Şehime G Temel, Liina Nagirnaja, et al.Pageof 2