Literature DB >> 2921039

Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27 beta (DXS255).

T Meitinger1, N A Fraser, B Lorenz, E Zrenner, J Murken, I W Craig.   

Abstract

A hypervariable DNA marker is closely linked to one of the most severe forms of night blindness, X-linked retinitis pigmentosa (RP). Affected individuals with X-linked RP, obligate carriers, and ophthalmologically identifiable carriers of the disease were included in a linkage study. The diagnosis was established in five sibships by funduscopic and electrophysiological investigations. When the X-linked probe M27 beta was used, 2 recombinants out of 29 informative meioses were detected (theta = 0.07 at a maximum lod of 4.75). The hypervariable probe detected two different alleles in 38 of 39 females tested. M27 beta is therefore a potentially very useful probe for carrier detection and prenatal diagnosis, as well as for addressing the question of heterogeneity of X-linked RP.

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Year:  1989        PMID: 2921039     DOI: 10.1007/BF00279005

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  19 in total

1.  X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome.

Authors:  U Friedrich; M Warburg; P Wieacker; T F Wienker; A Gal; H H Ropers
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  Variable number of tandem repeat (VNTR) markers for human gene mapping.

Authors:  Y Nakamura; M Leppert; P O'Connell; R Wolff; T Holm; M Culver; C Martin; E Fujimoto; M Hoff; E Kumlin
Journal:  Science       Date:  1987-03-27       Impact factor: 47.728

3.  Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7.

Authors:  M J Denton; J D Chen; S Serravalle; P Colley; F B Halliday; J Donald
Journal:  Hum Genet       Date:  1988-01       Impact factor: 4.132

4.  Report of the Committee on the Genetic Constitution of the X and Y Chromosomes.

Authors:  P N Goodfellow; K E Davies; H H Ropers
Journal:  Cytogenet Cell Genet       Date:  1985

5.  Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers.

Authors:  R L Nussbaum; R A Lewis; J G Lesko; R Ferrell
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

6.  Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

Authors:  N J Fraser; Y Boyd; G G Brownlee; I W Craig
Journal:  Nucleic Acids Res       Date:  1987-11-25       Impact factor: 16.971

7.  Genomic sequencing.

Authors:  G M Church; W Gilbert
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

8.  Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28.

Authors:  S S Bhattacharya; A F Wright; J F Clayton; W H Price; C I Phillips; C M McKeown; M Jay; A C Bird; P L Pearson; E M Southern
Journal:  Nature       Date:  1984 May 17-23       Impact factor: 49.962

9.  X-linked recessive retinitis pigmentosa. Clinical characteristics of carriers.

Authors:  G A Fishman; A B Weinberg; T T McMahon
Journal:  Arch Ophthalmol       Date:  1986-09

10.  Two highly polymorphic minisatellites from the pseudoautosomal region of the human sex chromosomes.

Authors:  M C Simmler; C Johnsson; C Petit; F Rouyer; G Vergnaud; J Weissenbach
Journal:  EMBO J       Date:  1987-04       Impact factor: 11.598

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  6 in total

1.  Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa.

Authors:  M Coleman; S Bhattacharya; S Lindsay; A Wright; M Jay; M Litt; I Craig; K Davies
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

2.  Risk calculation in retinitis pigmentosa.

Authors:  S M Holloway; L Strain; A E Shrimpton; A F Wright; M A Aldred; D Brosnahan; H Hammer; M Jay; D J Brock
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

3.  Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

Authors:  A F Wright; S S Bhattacharya; M A Aldred; M Jay; A D Carothers; N S Thomas; A C Bird; B Jay; H J Evans
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318

4.  X-inactivation pattern in carriers of X-linked retinitis pigmentosa: a valuable means of prognostic evaluation?

Authors:  U Friedrich; M Warburg; A L Jørgensen
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132

Review 5.  Organization of the human genome.

Authors:  I W Craig
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

6.  A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalities.

Authors:  D B van Dorp; A F Wright; A D Carothers; E M Bleeker-Wagemakers
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

  6 in total

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