X-linked albinism-deafness syndrome and Waardenburg syndrome type II: a hypothesis

Am J Med Genet. 1995 Nov 20;59(3):386-7. doi: 10.1002/ajmg.1320590321.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Albinism, Oculocutaneous / genetics*
  • Arm / abnormalities
  • DNA-Binding Proteins / genetics
  • Deafness / congenital
  • Deafness / genetics*
  • Female
  • Genes, Dominant
  • Humans
  • Infant, Newborn
  • Male
  • Models, Genetic*
  • PAX3 Transcription Factor
  • Paired Box Transcription Factors
  • Syndrome
  • Transcription Factors*
  • Waardenburg Syndrome / classification
  • Waardenburg Syndrome / genetics*
  • X Chromosome / genetics*

Substances

  • DNA-Binding Proteins
  • PAX3 Transcription Factor
  • PAX3 protein, human
  • Paired Box Transcription Factors
  • Transcription Factors
  • Pax3 protein, mouse