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Irradiation Hybrids for Human Chromosome 11: Characterization and Use for Generating Region-Specific Markers in 11q14-q23

โœ Scribed by G.T. Gillett; C.M. McConville; P.J. Byrd; T. Stankovic; A.M. Taylor; D.M. Hunt; L.F. West; M.F. Fox; S. Povey; F.J. Benham

Book ID
115611439
Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
639 KB
Volume
15
Category
Article
ISSN
0888-7543

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DiGeorge syndrome (DGS) is a human developmental defect of the structures derived from the third and fourth pharyngeal pouches. It apparently arises due to deletion of 22q11. We describe a strategy for the isolation of DNA probes for this region. A deleted chromosome 22, which includes 22q11, was fl