Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generations.

समान संसाधन

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