CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML).

Shiba, Norio

CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML). [electronic resource] - Blood Mar 2012 - 2612-4 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1528-0020

10.1182/blood-2011-02-333435 doi


Adult
Blood Platelet Disorders--complications
Child
Chromosomes, Human, Pair 11--genetics
Core Binding Factor Alpha 2 Subunit--genetics
Female
Genes, Dominant
Genetic Predisposition to Disease
Haplotypes--genetics
Humans
Immunoblotting
Leukemia, Myeloid, Acute--complications
Leukemia, Myelomonocytic, Chronic--etiology
Male
Middle Aged
Mutation--genetics
Pedigree
Polymerase Chain Reaction
Proto-Oncogene Proteins c-cbl--genetics