Cargando…
Chromosomal Aberrations in ETV6/RUNX1-positive Childhood Acute Lymphoblastic Leukemia using 244K Oligonucleotide Array Comparative Genomic Hybridization
BACKGROUND: Acute lymphoblastic leukemia (ALL) is a heterogeneous form of hematological cancer consisting of various subtypes. We are interested to study the genetic aberration in precursor B-cell ALL with specific t(12;21) translocation in childhood ALL patients. A high resolution 244K array-based...
Autores principales: | Zakaria, Zubaidah, Ahid, Mohd Fadly Md, Ismail, Azli, Keoh, Ten Sew, Nor, Nooraisyah Mohamad, Kamaluddin, Nor Rizan, Esa, Ezalia, Yuen, Lam Kah, Rahman, Eni Juraida Abdul, Osman, Raudhawati |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549777/ https://www.ncbi.nlm.nih.gov/pubmed/23151340 http://dx.doi.org/10.1186/1755-8166-5-41 |
Ejemplares similares
-
Whole-Exome Sequencing of ETV6/RUNX1 in Four Childhood Acute Lymphoblastic Leukaemia Cases
por: Zakaria, Zubaidah, et al.
Publicado: (2017) -
Comprehensive analysis of mutations and clonal evolution patterns in a cohort of patients with cytogenetically normal acute myeloid leukemia
por: Mat Yusoff, Yuslina, et al.
Publicado: (2021) -
Prevalence of BCR-ABL T315I Mutation in Malaysian Patients with Imatinib-Resistant Chronic Myeloid Leukemia
por: Yusoff, Yuslina Mat, et al.
Publicado: (2018) -
Identification of FLT3 and NPM1 Mutations in Patients with Acute Myeloid Leukaemia
por: Yusoff, Yuslina Mat, et al.
Publicado: (2019) -
Terminal microdeletion of chromosome 18 in a Malaysian boy characterized with few features of typical 18q- deletion syndrome: a case report
por: Ismail, Azli, et al.
Publicado: (2023)