CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML). [electronic resource]
Producer: 20120521Description: 2612-4 p. digitalISSN:- 1528-0020
- 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
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.