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
Rare germline variants in pancreatic cancer and multiple primary cancers: an autopsy study.
Fujitani H et al.
European Journal of Cancer Prevention : the Official Journal of the European Cancer Prevention Organisation (ecp), 2023
36896836 (PubMed )
Supplement: ejcp-32-286-s002.pdf
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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