Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q

Nat Genet. 1994 Apr;6(4):401-4. doi: 10.1038/ng0494-401.


Holt-Oram syndrome (HOS) is an autosomal dominant condition affecting the heart and upper limbs. We have sought to identify the location of this gene using microsatellite DNA markers in a linkage study. Of seven families analysed, five show linkage between HOS and markers on chromosome 12q. But the two remaining families, phenotypically indistinguishable from the others, do not show this linkage. Analysis with the computer program HOMOG indicates that HOS is a heterogeneous disease. Our analysis places one HOS locus in a 21 cM interval in the distal region of chromosome 12q. The localization of a gene for HOS, reported here, represents an important step towards a better understanding of limb and cardiac development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / classification
  • Abnormalities, Multiple / genetics*
  • Arm / abnormalities*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 12*
  • Crossing Over, Genetic
  • DNA, Satellite / genetics
  • Female
  • Genes, Dominant*
  • Genetic Markers
  • Hand Deformities, Congenital / classification
  • Hand Deformities, Congenital / genetics*
  • Heart Defects, Congenital / classification
  • Heart Defects, Congenital / genetics*
  • Humans
  • Male
  • Pedigree
  • Syndrome


  • DNA, Satellite
  • Genetic Markers