Holt-Oram syndrome with associated postaxial and central polydactyly. Further evidence for genetic heterogeneity in the Holt-Oram syndrome
Genet Couns
.
1996;7(4):323-4.
Authors
J P Fryns
,
D Bonnet
,
L De Smet
PMID:
8985738
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Chromosome Aberrations / genetics*
Chromosome Disorders
Chromosomes, Human, Pair 12
Female
Haplotypes
Humans
Infant
Pedigree
Phenotype
Polydactyly / genetics*
Syndrome