C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies. [electronic resource]
Producer: 20181211Description: 652-657 p. digitalISSN:- 1865-3774
- Biopsy
- Blood Platelet Disorders -- blood
- Child, Preschool
- Chromosome Aberrations
- Core Binding Factor Alpha 2 Subunit -- chemistry
- DNA Mutational Analysis
- Disease Progression
- Family
- Female
- Genetic Predisposition to Disease
- Humans
- Karyotype
- Leukemia, Myeloid -- diagnosis
- Mutation
- Platelet Count
- Polymorphism, Single Nucleotide
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Publication Type: Case Reports; Journal Article
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