Patients' age at time of testing for chromosome 22q11 microdeletions: missed opportunities for genetic counseling
Pediatr Cardiol
.
2000 Mar-Apr;21(2):183.
doi: 10.1007/s002469910034.
Authors
Y Liu
,
S Fallet
,
R Koppel
PMID:
10754096
DOI:
10.1007/s002469910034
No abstract available
Publication types
Letter
MeSH terms
Age Factors
Chromosome Deletion*
Chromosomes, Human, Pair 22*
Female
Heart Defects, Congenital / genetics*
Humans
In Situ Hybridization, Fluorescence*
Infant
Infant, Newborn
Male
Phenotype