Literature DB >> 2876947

Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimation.

J F Clayton, A F Wright, M Jay, C M McKeown, M Dempster, B S Jay, A C Bird, S S Bhattacharya.   

Abstract

Further linkage data relating X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28) is presented in this paper. The current mean estimate of the recombination fraction (theta) including this and all published data, is 0.09, with confidence limits 0.04 to 0.17 (maximum Lod score of 14.01 at a theta of 0.08). There is no evidence for heterogeneity of recombination fraction between the 13 families for which data are available. However, it is argued that heterogeneity should be assumed to exist for the purposes of risk estimation. Mean estimates and variances of risk are calculated for hypothetical families each with different linkage data. In families in which no recombination has been observed, the mean and variance of risk are sufficiently small for the clinical use of this probe to be acceptable to many.

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Year:  1986        PMID: 2876947     DOI: 10.1007/bf00282083

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


  13 in total

1.  TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS.

Authors:  C A SMITH
Journal:  Ann Hum Genet       Date:  1963-11       Impact factor: 1.670

2.  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

3.  Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

4.  Report of the Committee on Methods of Linkage Analysis and Reporting.

Authors:  P M Conneally; J H Edwards; K K Kidd; J M Lalouel; N E Morton; J Ott; R White
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.  An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy.

Authors:  J H Renwick; D R Bolling
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

7.  Linkage analysis and family classification under heterogeneity.

Authors:  J Ott
Journal:  Ann Hum Genet       Date:  1983-10       Impact factor: 1.670

8.  A genetic linkage study of a kindred with X-linked retinitis pigmentosa.

Authors:  S S Bhattacharya; J F Clayton; P S Harper; G W Hoare; M R Jay; A L Lyness; A F Wright
Journal:  Br J Ophthalmol       Date:  1985-05       Impact factor: 4.638

9.  Linkage between the X-linked retinitis pigmentosa locus and the L1.28 locus.

Authors:  S Mukai; T P Dryja; G A Bruns; J F Aldridge; E L Berson
Journal:  Am J Ophthalmol       Date:  1985-08-15       Impact factor: 5.258

10.  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

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  7 in total

1.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

2.  Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.

Authors:  M A Musarella; A Burghes; L Anson-Cartwright; M M Mahtani; R Argonza; L C Tsui; R Worton
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

3.  Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

Authors:  A F Wright; S S Bhattacharya; J F Clayton; M Dempster; P Tippett; C M McKeown; M Jay; B Jay; A C Bird
Journal:  Am J Hum Genet       Date:  1987-10       Impact factor: 11.025

4.  Recombination between DXS7, DXS84 and a rare form of X-linked retinitis pigmentosa (McK-30320).

Authors:  D Curtis; C E Blank
Journal:  Hum Genet       Date:  1989-01       Impact factor: 4.132

Review 5.  Diagnosis of genetic disease using recombinant DNA. Supplement.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

6.  Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests.

Authors:  J Ott; S Bhattacharya; J D Chen; M J Denton; J Donald; C Dubay; G J Farrar; G A Fishman; D Frey; A Gal
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

7.  Linkage heterogeneity and fragile X.

Authors:  J F Clayton; C M Gosden; N D Hastie; H J Evans
Journal:  Hum Genet       Date:  1988-04       Impact factor: 4.132

  7 in total

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