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Genes, Chromosomes & Cancer|December 28, 2020
Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemiaLarissa H Moura-Castro, Pablo Peña-Martínez, Anders Castor, et al.
Genes, Chromosomes & Cancer|February 24, 2015
A population-based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patientsVaidas Dirse, Agne Bertasiute, Egle Gineikiene, et al.
Genes, Chromosomes & Cancer|October 3, 2007
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemiaKajsa Paulsson, Andrea Horvat, Bodil Strömbeck, et al.
Genes, Chromosomes & Cancer|November 11, 2011
High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndromeCatarina Lundin, Lars Hjorth, Mikael Behrendtz, et al.
Cancers|March 27, 2019
Identification of Targetable Lesions in Anaplastic Thyroid Cancer by Genome ProfilingNaveen Ravi, Minjun Yang, Sigurdur Gretarsson, et al.
Oncotarget|November 7, 2015
Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemiaSetareh Safavi, Linda Olsson, Andrea Biloglav, et al.
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