Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generations.

Documenti analoghi

• Palmoplantar hyperkeratosis and deafness.
  di: Verbov, J
  Pubblicazione: (1992)
• A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)
  di: Heathcote, K., et al.
  Pubblicazione: (2000)
• Omphalocele in three generations with autosomal dominant transmission
  di: Kanagawa, S, et al.
  Pubblicazione: (2002)
• Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness
  di: Kenna, P., et al.
  Pubblicazione: (1997)
• Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report.
  di: Baraitser, M, et al.
  Pubblicazione: (1984)