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Different isoforms of the B-cell mutator activation-induced cytidine deaminase are aberrantly expressed in BCR-ABL1-positive acute lymphoblastic leukemia patients.
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Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.
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Genome-wide association study identifies three loci associated with melanoma risk.
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New common variants affecting susceptibility to basal cell carcinoma.
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Genome-wide profiling of genetic alterations in acute lymphoblastic leukemia: recent insights and future directions.
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A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups.
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A common allele on chromosome 9 associated with coronary heart disease.
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