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

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

Bibliographic Details
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/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412034/

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