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PMID: 3930157 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

In situ hybridization and translocation breakpoint mapping. III. DiGeorge syndrome with partial monosomy of chromosome 22.

Cytogenetics and cell genetics ·Vol. 39 ·No. 3 ·1985-00-00 ·Pages 179-83

Cannizzaro LA, Emanuel BS

Abstract

We have performed in situ hybridization of a probe for the lambda IGLC constant region to metaphase spreads from two DiGeorge syndrome (DGS)-related chromosomal rearrangements with breakpoints in 22q11. In this study we have demonstrated that the breakpoints are proximal to the lambda IGLC constant region cluster. Thus, at the molecular level, DGS-related breakpoints can be distinguished from the 22q11 breakpoint of CML, but not from the 8;22 translocation of Burkitt lymphoma or from the 21;22 translocations that we have previously studied.

MeSH Terms
Cell Line Chromosome Banding Chromosome Deletion Chromosome Mapping Chromosomes, Human, 21-22 and Y DiGeorge Syndrome/genetics Genes Humans Immunoglobulin Light Chains/genetics Immunoglobulin lambda-Chains/genetics Immunologic Deficiency Syndromes/genetics Karyotyping Monosomy Nucleic Acid Hybridization Translocation, Genetic
Chemicals
Immunoglobulin Light Chains Immunoglobulin lambda-Chains
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cannizzaro L A
Emanuel B S
Article Info
Journal
Cytogenetics and cell genetics
Abbr.
Cytogenet Cell Genet
ISSN
0301-0171
Published
1985-00-00
Pages
179-83
Language
English
Region
Switzerland
NLM ID
0367735
Subset
IM
Grants
NCI NIH HHS · CA-39926 · United States
NIGMS NIH HHS · GM-07511 · United States
NIGMS NIH HHS · GM-32592 · United States
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