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

โœ Scribed by Hirofumi Kobayashi; Rafael Espinosa III; Michael J. Thirman; Anthony A. Fernald; Kevin Shannon; Manuel O. Diaz; Michelle M. le Beau; Dr. Janet D. Rowley


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
376 KB
Volume
7
Category
Article
ISSN
1045-2257

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โœฆ Synopsis


Fluorescence in situ hybridization (FISH) was performed on bone marrow or peripheral blood cells thought to contain a del( I l)(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( I l)(q23) or del( I l)(q23q25) chromosomes may represent previously unidentified translocations that can be detected by FISH. Genes Chrorn Cancer 7: 204-208 (1993).


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Characterization of the breakpoints in a
โœ Olga Chernova; Ivan Still; Matt Kalaycio; Gerald Hoeltge; John K. Cowell ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 199 KB ๐Ÿ‘ 1 views

We used fluorescence in situ hybridization to characterize the molecular position of the breakpoints in a t(8;13)(p11;q12) reciprocal translocation from a patient with an atypical myeloproliferative disorder. This structural chromosome abnormality is characteristic of this specific disease and occur