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Molecular Cytogenetic Characterization of the DiGeorge Syndrome Region Using Fluorescence in Situ Hybridization

✍ Scribed by Elizabeth A. Lindsay; Stephanie Halford; Roy Wadey; Peter J. Scambler; Antonio Baldini

Book ID
115611706
Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
417 KB
Volume
17
Category
Article
ISSN
0888-7543

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In a series of ten patients affected by DiGeorge syndrome, we screened, by high resolution banding and fluorescent in situ hybridization of a cosmid probe, for microdeletions associated with this syndrome. In the ten patients, a microdeletion was demonstrated by in situ hybridization, but suspected