A cytogenetic study of familial deafness

J Med Genet. 1969 Sep;6(3):298-303. doi: 10.1136/jmg.6.3.298.
No abstract available

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Chromatids
  • Chromosome Aberrations
  • Chromosomes, Human, 16-18
  • Chromosomes, Human, 6-12 and X
  • Deafness / genetics*
  • Female
  • Humans
  • Infant
  • Karyotyping
  • Male
  • Pedigree