A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.

Hungate EA, Vora SR, Gamazon ER, Moriyama T, Best T, Hulur I, Lee Y, Evans TJ, Ellinghaus E, Stanulla M, Rudant J, Orsi L, Clavel J, Milne E, Scott RJ, Pui CH, Cox NJ, Loh ML, Yang JJ, Skol AD, Onel K
Nat Commun. 2016 7: 10635

PMID: 26868379 · PMCID: PMC4754340 · DOI:10.1038/ncomms10635

MeSH Terms (18)

African Americans Case-Control Studies Child Child, Preschool Chromosome Mapping Chromosomes, Human, Pair 9 Cyclin-Dependent Kinase Inhibitor p15 European Continental Ancestry Group Female Genetic Predisposition to Disease Genetic Variation Genome-Wide Association Study Hispanic Americans Humans Infant Male Polymorphism, Single Nucleotide Precursor B-Cell Lymphoblastic Leukemia-Lymphoma

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