Gene linkage and genetic deafness

C. W.R.J. Cremers, S. D.M. Brown, K. P. Steel, H. G. Brunner, A. P. Read, W. J. Kimberling

Research output: Contribution to journalArticle

5 Scopus citations
Original languageEnglish (US)
Pages (from-to)S167-S174
JournalInternational Journal of Pediatric Otorhinolaryngology
Volume32
DOIs
Publication statusPublished - Jan 1 1995

Keywords

  • Alport syndrome
  • Autosomal recessive congenital deafness
  • BOR-syn-drome
  • Gene linkage
  • Genetic deafness
  • Hereditary deafness
  • Stapes gusher syndrome
  • Treacher Collins syndrome
  • Usher syndrome
  • Waardenburg syndrome

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Otorhinolaryngology

Cite this

Cremers, C. W. R. J., Brown, S. D. M., Steel, K. P., Brunner, H. G., Read, A. P., & Kimberling, W. J. (1995). Gene linkage and genetic deafness. International Journal of Pediatric Otorhinolaryngology, 32, S167-S174. https://doi.org/10.1016/0165-5876(94)01154-P