Literature DB >> 1601428

Highly informative dinucleotide repeat polymorphism at the D11S29 locus on chromosome 11q23.

L Warnich1, I Groenewald, L Theart, A E Retief.   

Abstract

The informativeness of locus D11S29 as a genetic marker was improved by the identification of a highly polymorphic (GT)n repeat within the locus. Ten alleles were identified in parents of 40 Centre d'Etude du Polymorphisme Humain families and the polymorphism information content (PIC) was 0.77. The increased PIC value thus enables refinement of the linkage map of 11q23.

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Year:  1992        PMID： 1601428     DOI： 10.1007/bf00220560

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


  18 in total

1.  Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region.

Authors:  O Sanal; S Wei; T Foroud; U Malhotra; P Concannon; P Charmley; W Salser; K Lange; R A Gatti
Journal:  Am J Hum Genet       Date:  1990-11       Impact factor: 11.025

Review 2.  Report of the committee on the genetic constitution of chromosome 11.

Authors:  C Junien; V van Heyningen
Journal:  Cytogenet Cell Genet       Date:  1990

3.  Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms.

Authors:  R Williamson; A Bowcock; K Kidd; P Pearson; J Schmidtke; H S Chan; M Chipperfield; D N Cooper; J Hewitt; F Lewitter
Journal:  Cytogenet Cell Genet       Date:  1990

4.  An anonymous human single copy genomic clone, D11S29 (L7) at 11q23, identifies a moderately frequent RFLP.

Authors:  L Warnich; M J Kotze; A E Retief; E Dietzsch; M F Fox; G M Kotze; D L Nicholson; E Retief; C J Oosthuizen
Journal:  Nucleic Acids Res       Date:  1986-02-25       Impact factor: 16.971

5.  Five polymorphic microsatellite VNTRs on the human X chromosome.

Authors:  J A Luty; Z Guo; H F Willard; D H Ledbetter; S Ledbetter; M Litt
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

Review 6.  Report of the committee on the genetic constitution of chromosome 11.

Authors:  C Junien; O W McBride
Journal:  Cytogenet Cell Genet       Date:  1989

7.  Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred.

Authors:  D J Kwiatkowski; T G Nygaard; D E Schuback; S Perman; J M Trugman; S B Bressman; R E Burke; M F Brin; L Ozelius; X O Breakefield
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

8.  Comparative mapping of the constitutional and tumor-associated 11;22 translocations.

Authors:  M Budarf; B Sellinger; C Griffin; B S Emanuel
Journal:  Am J Hum Genet       Date:  1989-07       Impact factor: 11.025

9.  Genetic heterogeneity in tuberous sclerosis.

Authors:  L A Janssen; L A Sandkuyl; E C Merkens; J A Maat-Kievit; J R Sampson; P Fleury; R C Hennekam; G C Grosveld; D Lindhout; D J Halley
Journal:  Genomics       Date:  1990-10       Impact factor: 5.736

10.  Analysis of 7 polymorphic markers at chromosome 11q22-23 in 35 ataxia telangiectasia families; further evidence of linkage.

Authors:  C M McConville; C G Woods; M Farrall; J A Metcalfe; A M Taylor
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132
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  6 in total

1.  Bcl-2 expression in colorectal tumors: evidence of different pathways in sporadic and ulcerative-colitis-associated carcinomas.

Authors:  M Ilyas; I P Tomlinson; A M Hanby; T Yao; W F Bodmer; I C Talbot
Journal:  Am J Pathol       Date:  1996-11       Impact factor: 4.307

2.  A partial hydatidiform mole with 2N/3N mosaicism identified by molecular analysis.

Authors:  Y Ikeda; Y Jinno; H Masuzaki; N Niikawa; T Ishimaru
Journal:  J Assist Reprod Genet       Date:  1996-10       Impact factor: 3.412

3.  Chromosome 11q in sporadic colorectal carcinoma: patterns of allele loss and their significance for tumorigenesis.

Authors:  I P Tomlinson; W F Bodmer
Journal:  J Clin Pathol       Date:  1996-05       Impact factor: 3.411

4.  Allele loss occurs frequently at hMLH1, but rarely at hMSH2, in sporadic colorectal cancers with microsatellite instability.

Authors:  I P Tomlinson; M Ilyas; W F Bodmer
Journal:  Br J Cancer       Date:  1996-11       Impact factor: 7.640

5.  Loss of heterozygosity and amplification on chromosome 11q in human ovarian cancer.

Authors:  W D Foulkes; I G Campbell; G W Stamp; J Trowsdale
Journal:  Br J Cancer       Date:  1993-02       Impact factor: 7.640

6.  Loss of heterozygosity occurs at the D11S29 locus on chromosome 11q23 in invasive cervical carcinoma.

Authors:  P B Bethwaite; J Koreth; C S Herrington; J O McGee
Journal:  Br J Cancer       Date:  1995-04       Impact factor: 7.640
  6 in total

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