No parental origin bias for the rearranged chromosomes in myeloid leukemias associated with t(9;22), t(8;21) and t(15;17)
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Oncology,Hematology
Reference8 articles.
1. Parental origin of chromosomes involved in the translocation t(9;22);Haas;Nature,1992
2. Lack of imprinting of BCR;Riggins;Nat Genet,1994
3. No evidence for genomic imprinting of the human BCR gene;Fioretos;Blood,1994
4. Parental origin of the rearranged major breakpoint cluster region in chronic myeloid leukemia;Litz;Blood,1994
5. Lack of imprinting of the ABL gene;Melo;Nat Genet,1994
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The paternal chromosome 9 and the maternal chromosome 22 are preferentially rearranged in chronic myeloid leukaemia;Leukemia;2004-06-10
2. Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations;Journal of Medical Genetics;2003-09-01
3. Do Rosette, Heterochromatin, and/or Genomic Imprinting Influence Preferential Translocations in Human Neoplasia?;Cancer Genetics and Cytogenetics;2000-01
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