TY  - GEN
AU  - Tobias,E S
AU  - Morrison,N
AU  - Whiteford,M L
AU  - Tolmie,J L
TI  - Towards earlier diagnosis of 22q11 deletions
SN  - 1468-2044
PY  - 2000///0119
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 22
KW  - Craniofacial Abnormalities
KW  - DiGeorge Syndrome
KW  - genetics
KW  - Heart Defects, Congenital
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Tetralogy of Fallot
KW  - Time Factors
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1136/adc.81.6.513
ER  -