Associated Papers
Clinical syndromes linked to biallelic germline variants in MCM8 and MCM9.
Helderman NC et al.
Hgg Advances, 2025
40684266 (PubMed )
Supplement: mmc2.xlsx › Sheet1
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Identification of potential causal variants for premature ovarian failure by whole exome sequencing.
Jin H et al.
Bmc Medical Genomics, 2020
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