Literature DB >> 2016091

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

R Kumar-Singh1, D G Bradley, G J Farrar, M Lawler, S A Jordan, P Humphries.   

Abstract

We report the characterization of a new eight-allele microsatellite (D3S621) isolated from a human chromosome 3 library. Two-point and multi-locus genetic linkage analysis have shown D3S621 to co-segregate with the previously mapped RP4 (theta m = 0.12, Zm = 4.34) and with other genetic markers on the long arm of the chromosome, including D3S14 (R208) (theta m = 0.00, Zm = 15.10), D3S47 (C17) (theta m = 0.11, Zm = 4.95), Rho (theta m = 0.07, Zm = 1.37), D3S21 (L182) (theta m = 0.07, Zm = 2.40) and D3S19 (U1) (theta m = 0.13, Zm = 2.78). This highly informative marker, with a polymorphic information content of 0.78, should be of considerable value in the extension of linkage data for autosomal dominant retinitis pigmentosa with respect to locii on the long arm of chromosome 3.

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Year:  1991        PMID: 2016091     DOI: 10.1007/bf00194642

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


  22 in total

1.  A computer program to make linkage analysis with LIPED and LINKAGE easier to perform and less prone to input errors.

Authors:  J Attwood; S Bryant
Journal:  Ann Hum Genet       Date:  1988-07       Impact factor: 1.670

2.  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

3.  Non-Alu family interspersed repeats in human DNA and their transcriptional activity.

Authors:  L Sun; K E Paulson; C W Schmid; L Kadyk; L Leinwand
Journal:  Nucleic Acids Res       Date:  1984-03-26       Impact factor: 16.971

4.  Simple sequences are ubiquitous repetitive components of eukaryotic genomes.

Authors:  D Tautz; M Renz
Journal:  Nucleic Acids Res       Date:  1984-05-25       Impact factor: 16.971

5.  Two forms of autosomal dominant primary retinitis pigmentosa.

Authors:  R W Massof; D Finkelstein
Journal:  Doc Ophthalmol       Date:  1981-11       Impact factor: 2.379

6.  Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3.

Authors:  J E Olsson; C Samanns; J Jimenez; J Pongratz; A Chand; A Watty; S A Seuchter; M Denton; A Gal
Journal:  Am J Med Genet       Date:  1990-04

7.  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

Review 8.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Authors:  D Botstein; R L White; M Skolnick; R W Davis
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

9.  Autosomal dominantly inherited retinitis pigmentosa. Visual acuity loss by subtype.

Authors:  M D Farber; G A Fishman; R A Weiss
Journal:  Arch Ophthalmol       Date:  1985-04

10.  A study of retinitis pigmentosa in the City of Birmingham. I Prevalence.

Authors:  S Bundey; S J Crews
Journal:  J Med Genet       Date:  1984-12       Impact factor: 6.318

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  2 in total

1.  Autosomal dominant retinitis pigmentosa: no evidence for nonallelic genetic heterogeneity on 3q.

Authors:  R Kumar-Singh; H Wang; P Humphries; G J Farrar
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

2.  Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locus.

Authors:  R Kumar-Singh; S A Jordan; G J Farrar; P Humphries
Journal:  Nucleic Acids Res       Date:  1991-10-25       Impact factor: 16.971

  2 in total

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