Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia

Documenti analoghi

• Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia
  di: Gunnarsson, Rebeqa, et al.
  Pubblicazione: (2018)
• Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A
  di: Karrman, Kristina, et al.
  Pubblicazione: (2015)
• Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia
  di: Lundin-Ström, Kristina B., et al.
  Pubblicazione: (2020)
• Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia
  di: Lilljebjörn, Henrik, et al.
  Pubblicazione: (2016)
• Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia
  di: Safavi, Setareh, et al.
  Pubblicazione: (2015)