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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

Crossref DOI link: https://doi.org/10.1186/s13045-015-0138-0

Published Online: 2015-04-24

Published Print: 2015-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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