Chromosomal Aberrations During Progression of Chronic Myeloid Leukemia Identified by Cytogenetic and Molecular Cytogenetic Tools
- 1 January 1999
- journal article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 108 (1) , 6-12
- https://doi.org/10.1016/s0165-4608(98)00120-4
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Increasing methylation of the calcitonin gene during disease progression in sequential samples from CML patientsLeukemia Research, 1996
- The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9Nature Genetics, 1996
- Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemiaNature Genetics, 1996
- Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroupsGenes, Chromosomes and Cancer, 1995
- Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumorsGenes, Chromosomes and Cancer, 1994
- Karyotypic findings as an independent prognostic marker in chronic myeloid leukaemia blast crisisLeukemia Research, 1994
- Direct visualization of the transposedABL gene in a duplicated masked Ph chromosomeGenes, Chromosomes and Cancer, 1993
- Differences Between Blastic Chronic Myeloid Leukemia and Ph-Positive Acute LeukemiaLeukemia & Lymphoma, 1993
- Molecular Defects Associated with the Acute Phase CMLLeukemia & Lymphoma, 1993
- The spectrum of molecular alterations in the evolution of chronic myelocytic leukemia.Journal of Clinical Investigation, 1991