Literature DB >> 2564733

Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locus.

D G Bradley1, G J Farrar, E M Sharp, P Kenna, M M Humphries, D J McConnell, S P Daiger, P McWilliam, P Humphries.   

Abstract

Members of a large Irish pedigree exhibiting early-onset autosomal dominant retinitis pigmentosa (ADRP) were typed for the rhesus blood group and nine DNA markers on chromosome 1. Close linkage between the ADRP locus and any of the marker loci was excluded using two-point analysis. With use of the sex-averaged maps of Dracopoli et al. and Donis-Keller et al. and a strategy of rolling multipoint analyses, support was gained for the exclusion of ADRP from a 224-cM region of the chromosome, including almost the entire short arm. The disease locus was significantly excluded from within at least 50 cM of the rhesus locus and, as a loose linkage between these two genes has been suggested by other studies, this result may support the possibility of genetic heterogeneity within the autosomal dominant subgroup of retinitis pigmentosa.

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Year:  1989        PMID: 2564733      PMCID: PMC1715578     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  29 in total

1.  Sequential tests for the detection of linkage.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1955-09       Impact factor: 11.025

2.  Report of the committee on the genetic constitution of the X and Y chromosomes.

Authors:  K E Davies; J L Mandel; J Weissenbach; M Fellous
Journal:  Cytogenet Cell Genet       Date:  1987

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Authors:  N E Morton; G A Bruns
Journal:  Cytogenet Cell Genet       Date:  1987

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Authors:  H Donis-Keller; P Green; C Helms; S Cartinhour; B Weiffenbach; K Stephens; T P Keith; D W Bowden; D R Smith; E S Lander
Journal:  Cell       Date:  1987-10-23       Impact factor: 41.582

5.  Problems in detecting etiological heterogeneity in genetic disease illustrated with retinitis pigmentosa.

Authors:  T H Beaty; J A Boughman
Journal:  Am J Med Genet       Date:  1986-07

6.  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

7.  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

8.  Electroretinography and retinitis pigmentosa. No discrimination between genetic subtypes.

Authors:  D S Rothberg; G W Weinstein; R R Hobson; T M Nork
Journal:  Arch Ophthalmol       Date:  1982-09

9.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

10.  Structural gene for beta-nerve growth factor not defective in familial dysautonomia.

Authors:  X O Breakefield; G Orloff; C Castiglione; L Coussens; F B Axelrod; A Ullrich
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

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  2 in total

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

Authors:  C F Inglehearn; S S Papiha; M Jay; A F Wright; A T Moore; S S Bhattacharya
Journal:  J Med Genet       Date:  1990-01       Impact factor: 6.318

2.  Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4).

Authors:  R Kumar-Singh; D G Bradley; G J Farrar; M Lawler; S A Jordan; P Humphries
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

  2 in total

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