The mutation spectrum in Holt-Oram syndrome

J Med Genet. 2000 Oct;37(10):785-7. doi: 10.1136/jmg.37.10.785.
No abstract available

Publication types

  • Letter

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 12 / genetics
  • DNA Mutational Analysis
  • Exons / genetics
  • Female
  • Genetic Testing
  • Genetic Variation / genetics
  • Genotype
  • Heart Block / genetics
  • Heart Defects, Congenital / genetics*
  • Heart Septal Defects / genetics
  • Humans
  • Introns / genetics
  • Limb Deformities, Congenital / genetics*
  • Male
  • Molecular Sequence Data
  • Mutation / genetics*
  • Pedigree
  • Phenotype
  • Polymorphism, Single-Stranded Conformational
  • Syndactyly / genetics
  • Syndrome

Associated data

  • GENBANK/AF221714