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- W4385665095 abstract "Molecular and sequencing advances have led to substantial breakthroughs in the discovery of new genes and inherited mutations associated with increased risk of developing myeloid malignancies . Many of the same germline mutated genes are also drivers of malignancy in sporadic cancer. Recognition of myeloid malignancy associated with germline mutations is essential for proper therapy, disease surveillance, informing related donor selection for hematopoietic stem cell transplantation , and genetic counseling of the patient and affected family members. Some germline mutations are associated with syndromic features that precede the development of malignancy; however, penetrance may be highly variable leading to masking of the syndromic phenotype and/or inherited etiology." @default.
- W4385665095 created "2023-08-09" @default.
- W4385665095 creator A5020253470 @default.
- W4385665095 creator A5044681793 @default.
- W4385665095 creator A5081779514 @default.
- W4385665095 date "2023-08-01" @default.
- W4385665095 modified "2023-10-12" @default.
- W4385665095 title "Germline Predisposition to Myeloid Neoplasms" @default.
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- W4385665095 doi "https://doi.org/10.1016/j.cll.2023.06.004" @default.
- W4385665095 hasPublicationYear "2023" @default.
- W4385665095 type Work @default.