TY  - GEN
AU  - Smith,A
AU  - Robson,L
TI  - Low frequency of inherited deletions of 22q11
SN  - 0148-7299
PY  - 1999///0830
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 22
KW  - DiGeorge Syndrome
KW  - genetics
KW  - Female
KW  - Genetic Diseases, Inborn
KW  - Genetic Markers
KW  - Heart Defects, Congenital
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Male
KW  - Syndrome
KW  - Velopharyngeal Insufficiency
N1  - Publication Type: Letter
UR  - https://doi.org/10.1002/(sici)1096-8628(19990827)85:5<513::aid-ajmg16>3.0.co;2-j
ER  -