A locus for autosomal dominant keratoconus maps to human chromosome 3p14–q13

Podobne zapisy

• Autosomal dominant hereditary benign telangiectasia maps to the CMC1 locus for capillary malformation on chromosome 5q14
  od: Brancati, F, i wsp.
  Wydane: (2003)
• A novel locus for autosomal dominant non‐syndromic deafness, DFNA53, maps to chromosome 14q11.2‐q12
  od: Yan, D, i wsp.
  Wydane: (2006)
• Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12
  od: Flex, E, i wsp.
  Wydane: (2003)
• Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.
  od: Hedera, P, i wsp.
  Wydane: (1999)
• Investigation of a Family with Autosomal Dominant Dilated Cardiomyopathy Defines a Novel Locus on Chromosome 2q14-q22
  od: Jung, Martin, i wsp.
  Wydane: (1999)