Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus.

Podobne zapisy

• Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity.
  od: Lester, D H, i wsp.
  Wydane: (1990)
• Loci for autosomal dominant retinitis pigmentosa and dominant cystoid macular dystrophy on chromosome 7p are not allelic.
  od: Inglehearn, C., i wsp.
  Wydane: (1994)
• Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa families.
  od: Keen, T J, i wsp.
  Wydane: (1997)
• A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.
  od: Inglehearn, C F, i wsp.
  Wydane: (1991)
• Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression.
  od: Kim, R Y, i wsp.
  Wydane: (1995)