Associated Papers
DNA double-strand break genetic variants in patients with premature ovarian insufficiency.
Ding X et al.
Journal of Ovarian Research, 2023
The landscape of genetic variations in non-syndromic primary ovarian insufficiency in the MENA region: a systematic review.
Allouch A et al.
Frontiers in Endocrinology, 2023
Biallelic mutations in PSMC3IP are associated with secondary amenorrhea: expanding the spectrum of premature ovarian insufficiency.
Sirchia F et al.
Journal of Assisted Reproduction and Genetics, 2022
Two novel biallelic mutations in PSMC3IP in a patient affected by premature ovarian insufficiency.
Mei L et al.
Molecular Medicine Reports, 2022
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Meiotic Recombination Defects and Premature Ovarian Insufficiency.
Huang C et al.
Frontiers in Cell and Developmental Biology, 2021
Gene variants identified by whole-exome sequencing in 33 French women with premature ovarian insufficiency.
Yang X et al.
Journal of Assisted Reproduction and Genetics, 2019
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