DFNA25, a Novel Locus for Dominant Nonsyndromic Hereditary Hearing Impairment, Maps to 12q21-24

Ítems similars

• A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p.
  per: Brown, M R, et al.
  Publicat: (1997)
• A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration.
  per: Lalwani, A K, et al.
  Publicat: (1999)
• A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus
  per: Van Camp, G., et al.
  Publicat: (1999)
• A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.
  per: Verhoeven, K, et al.
  Publicat: (1997)
• A Novel Locus (DFNA24) for Prelingual Nonprogressive Autosomal Dominant Nonsyndromic Hearing Loss Maps to 4q35-qter in a Large Swiss German Kindred
  per: Häfner, Franziska M., et al.
  Publicat: (2000)