Direct familial transmission of the Turner phenotype

Am J Dis Child. 1968 Oct;116(4):343-50. doi: 10.1001/archpedi.1968.02100020347001.
No abstract available

MeSH terms

  • Chromosome Aberrations
  • Chromosome Disorders
  • Dermatoglyphics
  • Female
  • Heart Defects, Congenital / complications
  • Humans
  • Male
  • Pedigree
  • Phenotype*
  • Sex Chromatin
  • Sex Factors
  • Turner Syndrome / genetics*