Associated Papers
Case Report and Literature Review: A 46,XX Infant with Atypical Genitalia Diagnosed with Primary Ovarian Insufficiency Caused by HFM1 Gene Variants.
Yuan Z et al.
Hormone Research in Paediatrics, 2025
Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos.
Tang F et al.
Journal of Assisted Reproduction and Genetics, 2023
Novel pathogenic splicing variants in helicase for meiosis 1 (HFM1) are associated with diminished ovarian reserve and poor pregnancy outcomes.
Yu L et al.
Journal of Assisted Reproduction and Genetics, 2022
Association analysis between HFM1 variation and primary ovarian insufficiency in Chinese women.
Pu D et al.
Clinical Genetics, 2016
Mutations in HFM1 in recessive primary ovarian insufficiency.
Wang J et al.
The New England Journal of Medicine, 2014
Genetics of primary ovarian insufficiency: new developments and opportunities.
Qin Y et al.
Human Reproduction Update, 0
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