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.
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