TY  - GEN
AU  - Fryns,J P
AU  - Bonnet,D
AU  - De Smet,L
TI  - Holt-Oram syndrome with associated postaxial and central polydactyly. Further evidence for genetic heterogeneity in the Holt-Oram syndrome
SN  - 1015-8146
PY  - 1997///0318
KW  - Chromosome Aberrations
KW  - genetics
KW  - Chromosome Disorders
KW  - Chromosomes, Human, Pair 12
KW  - Female
KW  - Haplotypes
KW  - Humans
KW  - Infant
KW  - Pedigree
KW  - Phenotype
KW  - Polydactyly
KW  - Syndrome
N1  - Publication Type: Case Reports; Letter
ER  -