Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion
Am J Med Genet
.
1996 Aug 23;64(3):525-6.
doi: 10.1002/ajmg.1320640304.
Authors
D M McDonald-McGinn
,
B S Emanuel
,
E H Zackai
PMID:
8862635
DOI:
10.1002/ajmg.1320640304
No abstract available
Publication types
Comment
Letter
MeSH terms
Abnormalities, Multiple / genetics*
Chromosome Aberrations / genetics*
Chromosome Deletion*
Chromosome Disorders
Chromosomes, Human, Pair 22 / genetics*
Female
Genes, Dominant
Humans
Male
Syndrome