Smith-Magenis syndrome and tetralogy of Fallot
J Med Genet
.
1999 Jun;36(6):501-2.
Authors
E Sweeney
,
I Peart
,
M Tofeig
,
B Kerr
PMID:
10874646
PMCID:
PMC1734392
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Abnormalities, Multiple / genetics*
Chromosome Deletion
Chromosomes, Human, Pair 17 / genetics
Developmental Disabilities / genetics
Female
Humans
Infant
Male
Syndrome
Tetralogy of Fallot / genetics*