TY  - GEN
AU  - Goldmuntz,E
AU  - Driscoll,D
AU  - Budarf,M L
AU  - Zackai,E H
AU  - McDonald-McGinn,D M
AU  - Biegel,J A
AU  - Emanuel,B S
TI  - Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects
SN  - 0022-2593
PY  - 1993///1220
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Blotting, Southern
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 22
KW  - Cleft Palate
KW  - DiGeorge Syndrome
KW  - Gene Deletion
KW  - Heart Defects, Congenital
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Infant
KW  - Polymorphism, Restriction Fragment Length
KW  - Syndrome
KW  - Velopharyngeal Insufficiency
N1  - Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1136/jmg.30.10.807
ER  -