Associated Papers
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Genetic control of meiosis surveillance mechanisms in mammals.
Huang Y et al.
Frontiers in Cell and Developmental Biology, 2023
36910159 (PubMed )
Supplement: DataSheet2.PDF
Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia.
Xie C et al.
Human Reproduction Update, 2022
Identification of pathogenic mutations from nonobstructive azoospermia patients†.
Jiang H et al.
Biology of Reproduction, 2022
In silico analysis of a novel pathogenic variant c.7G > A in C14orf39 gene identified by WES in a Pakistani family with azoospermia.
Ali H et al.
Molecular Genetics and Genomics : Mgg, 2022
Alterations in synaptonemal complex coding genes and human infertility.
Zhang F et al.
International Journal of Biological Sciences, 2022
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Fan S et al.
American Journal of Human Genetics, 2021
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