A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies-Reference-Cited by-同舟云学术

A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies

Published:2005-12 Issue:2 Volume:163 Page:176-179
ISSN:0165-4608
Container-title:Cancer Genetics and Cytogenetics
language:en
Short-container-title:Cancer Genetics and Cytogenetics

Author:

MacKinnon Ruth N.,Campbell Lynda J.

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference11 articles.

1. The prognostic significance of deletion of the long arm of chromosome 20 in myeloid disorders;Campbell;Leukemia,1994

2. Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes;Bench;Oncogene,2000

3. Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies;Li;Proc Natl Acad Sci USA,2004

4. Identification of multiple copies of a 20q− chromosome in a case of myelodysplastic syndrome: a FISH study;Falzetti;Leuk Res,1999

5. An international system for human cytogenetics nomenclature;ISCN,1995

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