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Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population

BiologyAllelic VariantGenetic DisorderGeneticsGenetic EpidemiologyMolecular GeneticsGenetic VariationNbn MutationMedical GeneticsChildhood AllMedicineVariant InterpretationPolish Population