TY  - GEN
AU  - Driscoll,D A
TI  - Prenatal diagnosis of the 22q11.2 deletion syndrome
SN  - 1098-3600
PY  - 2001///0927
KW  - Abnormalities, Multiple
KW  - Adult
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 22
KW  - DiGeorge Syndrome
KW  - diagnosis
KW  - Facies
KW  - Female
KW  - Gene Deletion
KW  - Genetic Counseling
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - methods
KW  - Male
KW  - Phenotype
KW  - Polymerase Chain Reaction
KW  - Prenatal Diagnosis
KW  - Risk Factors
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.; Review
UR  - https://doi.org/10.1097/00125817-200101000-00004
ER  -