Literature DB >> 3783618

A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.

B Wainwright, M Farrall, E Watson, R Williamson.   

Abstract

We have used multilocus analysis to exclude the cystic fibrosis locus from six polymorphic DNA markers covering most of chromosome 19. A substantial increase in the confidence for exclusion was obtained using the computer programme LINKAGE compared to analysis of pairwise lod scores. A structured approach to the analysis of linkage to autosomal recessive inherited diseases where the biochemical defect is not known is described.

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Year:  1986        PMID: 3783618      PMCID: PMC1049778          DOI: 10.1136/jmg.23.5.417

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  27 in total

1.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

2.  Isolation and sequence of a human cytochrome P-450 cDNA clone.

Authors:  I R Phillips; E A Shephard; A Ashworth; B R Rabin
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

3.  Possible localisation of the gene for cystic fibrosis of the pancreas to the short arm of chromosome 5.

Authors:  D W Smith; J M Docter; P E Ferrier; J L Frias; A Spock
Journal:  Lancet       Date:  1968-08-10       Impact factor: 79.321

4.  Incidence in Italy, genetic heterogeneity, and segregation analysis of cystic fibrosis.

Authors:  G Romeo; M Bianco; M Devoto; P Menozzi; G Mastella; A M Giunta; C Micalizzi; M Antonelli; A Battistini; F Santamaria
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025

5.  Somatic cell genetic studies of the cystic fibrosis mucociliary inhibitor.

Authors:  B J Mayo; R J Klebe; D R Barnett; B J Lankford; B H Bowman
Journal:  Clin Genet       Date:  1980-11       Impact factor: 4.438

6.  Localisation of genetic markers and orientation of the linkage group on chromosome 19.

Authors:  J D Brook; D J Shaw; L Meredith; G A Bruns; P S Harper
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis.

Authors:  P Scambler; T Robbins; C Gilliam; A Boylston; P Tippett; R Williamson; K E Davies
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  A DNA polymorphism adjacent to the human apolipoprotein CII gene.

Authors:  S E Humphries; N I Jowett; L Williams; A Rees; M Vella; A Kessling; O Myklebost; A Lydon; M Seed; D J Galton
Journal:  Mol Biol Med       Date:  1983-12

9.  Cystic fibrosis is not caused by a defect in the gene coding for human complement C3.

Authors:  K E Davies; T C Gilliam; R Williamson
Journal:  Mol Biol Med       Date:  1983-09

10.  Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis.

Authors:  M Knowles; J Gatzy; R Boucher
Journal:  N Engl J Med       Date:  1981-12-17       Impact factor: 91.245

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  8 in total

1.  Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1.

Authors:  S Kumar; W J Kimberling; P A Gabow; Y Y Shugart; S Pieke-Dahl
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

2.  Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis.

Authors:  T Alitalo; T A Kruse; H Forsius; A W Eriksson; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

3.  Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).

Authors:  P Raeymaekers; V Timmerman; P De Jonghe; L Swerts; J Gheuens; J J Martin; L Muylle; G De Winter; A Vandenberghe; C Van Broeckhoven
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

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

Authors:  D G Bradley; G J Farrar; E M Sharp; P Kenna; M M Humphries; D J McConnell; S P Daiger; P McWilliam; P Humphries
Journal:  Am J Hum Genet       Date:  1989-04       Impact factor: 11.025

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.  Exclusion of the Friedreich ataxia gene from chromosome 19.

Authors:  S Chamberlain; C S Worrall; S South; J Shaw; M Farrall; R Williamson
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

7.  Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.

Authors:  A M Bowcock; L A Farrer; L L Cavalli-Sforza; J M Hebert; K K Kidd; M Frydman; B Bonne-Tamir
Journal:  Am J Hum Genet       Date:  1987-07       Impact factor: 11.025

8.  An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.

Authors:  L A Farrer; P J Goodfellow; C M Lamarche; I Franjkovic; S Myers; B N White; J J Holden; J R Kidd; N E Simpson; K K Kidd
Journal:  Am J Hum Genet       Date:  1987-04       Impact factor: 11.025

  8 in total

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