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
Main Authors: | Karrman, Kristina, Castor, Anders, Behrendtz, Mikael, Forestier, Erik, Olsson, Linda, Ehinger, Mats, Biloglav, Andrea, Fioretos, Thoas, Paulsson, Kajsa, Johansson, Bertil |
---|---|
Format: | Online |
Language: | English |
Published: |
BioMed Central
2015
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412034/ |
Similar Items
-
Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia
by: Safavi, Setareh, et al.
Published: (2015) -
Paternal Uniparental Isodisomy of Chromosome 11p15.5 within the Pancreas Causes Isolated Hyperinsulinemic Hypoglycemia
by: Flanagan, S. E., et al.
Published: (2011) -
Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome
by: Benjamin M. Helm, et al.
Published: (2017-07-01) -
Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy
by: Kocaay, Pınar, et al.
Published: (2016) -
Diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy
by: Bug, Stefanie, et al.
Published: (2014)