Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes. [electronic resource]
Producer: 20120210Description: 1462-9 p. digitalISSN:- 1592-8721
- Adolescent
- Adult
- Alleles
- Child
- Child, Preschool
- Female
- Genetic Association Studies
- Genotype
- Humans
- Infant
- Infant, Newborn
- Karyotyping
- Male
- Mutation
- Myeloproliferative Disorders -- genetics
- Phenotype
- Polycythemia Vera -- genetics
- Polymorphism, Single Nucleotide
- Primary Myelofibrosis -- diagnosis
- Repressor Proteins -- genetics
- Thrombocythemia, Essential -- genetics
- Thrombocytosis -- genetics
- Young Adult
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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