Holt-Oram syndrome: penetrance of the gene and lack of maternal effect

Clin Genet. 1982 Feb;21(2):98-103. doi: 10.1111/j.1399-0004.1982.tb00743.x.
No abstract available

MeSH terms

  • Adolescent
  • Adult
  • Extrachromosomal Inheritance*
  • Female
  • Genes, Dominant
  • Genetic Variation*
  • Hand Deformities, Congenital*
  • Heart Defects, Congenital / genetics*
  • Humans
  • Male
  • Pedigree
  • Phenotype
  • Syndrome