Sort   by:  
 Page size 
UnknownAXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.
Not available
S-EPMC10107344 | biostudies-literature
UnknownGene- and pathway-level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility.
Not available
S-EPMC9290690 | biostudies-literature
UnknownScreening Mammography and Breast Cancer: Variation in Risk with Rare Deleterious or Predicted Deleterious Variants in DNA Repair Genes.
Not available
S-EPMC11987804 | biostudies-literature
UnknownDiagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation.
Not available
S-EPMC8336294 | biostudies-literature
UnknownFamilial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing.
Not available
S-EPMC6587727 | biostudies-literature
UnknownNull and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans.
Not available
S-EPMC10357479 | biostudies-literature
UnknownClassification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.
Not available
S-EPMC8546044 | biostudies-literature
Sort   by:  
 Page size