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Query Trace: Azoospermia and USP9Y[orginal query]

Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure. Asian journal of andrology 2020 Jul . Cannarella Rossella, Condorelli Rosita A, Paolacci Stefano, Barbagallo Federica, Guerri Giulia, Bertelli Matteo, La Vignera Sandro, Calogero Aldo Similar articles in PubMed
Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment. Human reproduction (Oxford, England) 2008 Sep 23 (9): 2167-72. Yang Yuan, Ma Mingyi, Li Lei, Zhang Wei, Chen Pu, Ma Yongxin, Liu Yunqiang, Tao Dachang, Lin Li, Zhang Sizho Similar articles in PubMed
Study of azoospermia factor-a deletion caused by homologous recombination between the human endogenous retroviral elements and population-specific alleles in Japanese infertile males. Fertility and sterility 2008 May 89 (5): 1177-82. Choi Jin, Koh Eitetsu, Matsui Fotoshi, Sugimoto Kazuhiro, Suzuki Hiromi, Maeda Yuji, Yoshida Atsumi, Namiki Mik Similar articles in PubMed
Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermia. Molecular human reproduction 2005 Sep 11 (9): 673-5. Westerveld G H, Repping S, Lombardi M P, van der Veen Similar articles in PubMed