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Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family

Published in: Human Genetics

Date of publication: January 1, 1995

Main subject: retinitis pigmentosa

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Cites articles 19

Date

Title

Authors

March 1, 1988

Efficient computations in multilocus linkage analysis

,
October 1, 1989

Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3
March 1, 1989

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
January 1990

Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests
December 1, 1991

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.
October 1, 1991

Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locus
March 1992

Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin
October 1, 1992

A second-generation linkage map of the human genome
July 1992

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13
June 1, 1992

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa
May 1, 1993

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q

,
June 1, 1993

Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa
July 1, 1993

Faster sequential genetic linkage computations
January 1, 1993

A leucine to arginine amino acid substitution at codon 46 of rhodopsin is responsible for a severe form of autosomal dominant retinitis pigmentosa
June 1993

(CA)n-dinucleotide repeat at the PDEB locus in 4p16.3
May 1, 1993

A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.
July 1, 1993

Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8).
February 1994

Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19
June 1994

The 1993-94 Généthon human genetic linkage map,The 1993–94 Généthon human genetic linkage map

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