Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village.

Lignende værker

• Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction
  af: Naz, S, et al.
  Udgivet: (2004)
• Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness
  af: Ben-Yosef, T., et al.
  Udgivet: (2001)
• Autosomal recessive nonsyndromic deafness genes: a review
  af: Duman, Duygu, et al.
  Udgivet: (2012)
• A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism.
  af: Edwards, B D, et al.
  Udgivet: (1989)
• Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome.
  af: Santos, H, et al.
  Udgivet: (1988)