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PMID: 7692945 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization.

Genes, chromosomes & cancer ·Vol. 7 ·No. 4 ·1993-08-00 ·Pages 204-8

Kobayashi H, Espinosa R, Thirman MJ, Fernald AA, Shannon K, Diaz MO, Le Beau MM, Rowley JD

Abstract

Fluorescence in situ hybridization (FISH) was performed on bone marrow or peripheral blood cells thought to contain a del(11)(q23q25) from four patients who had acute leukemia or myelodysplasia. Cells from all patients were shown to contain translocations that involved chromosome 6 in three of them. Our data suggest that a large proportion of presumptive del(11)(q23) or del(11)(q23q25) chromosomes may represent previously unidentified translocations that can be detected by FISH.

MeSH Terms
Acute Disease Adolescent Adult Aged Child Chromosome Deletion Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 6 Female Humans In Situ Hybridization, Fluorescence Karyotyping Leukemia/genetics Male Myelodysplastic Syndromes/genetics Translocation, Genetic
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Kobayashi H
Department of Medicine, University of Chicago, Illinois 60637.
Espinosa R
Thirman M J
Fernald A A
Shannon K
Diaz M O
Le Beau M M
Rowley J D
Article Info
Journal
Genes, chromosomes & cancer
Abbr.
Genes Chromosomes Cancer
ISSN
1045-2257
Published
1993-08-00
Pages
204-8
Language
English
Region
United States
NLM ID
9007329
Subset
IM
Grants
NCI NIH HHS · CA 40046 · United States
NCI NIH HHS · CA38725 · United States
NCI NIH HHS · CA42577 · United States
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