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This dataset contains one vcf file with variants from whole exome sequencing of 24 paediatric AML samples at diagnosis.
Analysis of rare germline variants in childhood AML in a large panel of cancer predisposition genes (n=216) compiled from literature review, and including genes involved in familial hematological malignancies (HM) and bone marrow failure (BMF) syndromes. The prevalence of extremely rare variants in ...
Data Access Committee EGAC00001002686
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