Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects. [electronic resource]
Producer: 19931220Description: 807-12 p. digitalISSN:- 0022-2593
- Abnormalities, Multiple -- genetics
- Blotting, Southern
- Chromosome Deletion
- Chromosomes, Human, Pair 22
- Cleft Palate -- genetics
- DiGeorge Syndrome -- genetics
- Gene Deletion
- Heart Defects, Congenital -- genetics
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Polymorphism, Restriction Fragment Length
- Syndrome
- Velopharyngeal Insufficiency -- genetics
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Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
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