TY  - GEN
AU  - Staňo Kozubík,Kateřina
AU  - Radová,Lenka
AU  - Pešová,Michaela
AU  - Réblová,Kamila
AU  - Trizuljak,Jakub
AU  - Plevová,Karla
AU  - Fiamoli,Veronika
AU  - Gumulec,Jaromír
AU  - Urbánková,Helena
AU  - Szotkowski,Tomáš
AU  - Mayer,Jiří
AU  - Pospíšilová,Šárka
AU  - Doubek,Michael
TI  - C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies
SN  - 1865-3774
PY  - 2018///1211
KW  - Biopsy
KW  - Blood Platelet Disorders
KW  - blood
KW  - Child, Preschool
KW  - Chromosome Aberrations
KW  - Core Binding Factor Alpha 2 Subunit
KW  - chemistry
KW  - DNA Mutational Analysis
KW  - Disease Progression
KW  - Family
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - Karyotype
KW  - Leukemia, Myeloid
KW  - diagnosis
KW  - Mutation
KW  - Platelet Count
KW  - Polymorphism, Single Nucleotide
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1007/s12185-018-2514-3
ER  -