Dual transcription of b2a2 and b3a2 BCR-ABL transcripts in chronic myeloid leukaemia is confined to patients with a linked polymorphism within the BCR gene

Author:

Branford Susan,Hughes Timothy P.,Rudzki Zbigniew

Publisher

Wiley

Subject

Hematology

Reference11 articles.

1. Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group;Antonarakis;Human Mutation,1998

2. Monitoring chronic myeloid leukaemia therapy by real-time quantitative PCR in blood is a reliable alternative to bone marrow cytogenetics;Branford;British Journal of Haematology,1999

3. Sequence and analysis of the human ABL gene, the BCR gene, and regions involved in the Philadelphia chromosomal translocation;Chissoe;Genomics,1995

4. A polymorphism in exon b2 of the major breakpoint cluster region (M-bcr) identified in chronic myeloid leukaemia patients;Meissner;British Journal of Haematology,1998

5. Parental somatic and germ-line mosaicism for a FBN2 mutation and analysis of FBN2 transcript levels in dermal fibroblasts;Putnam;American Journal of Human Genetics,1997

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