Literature DB >> 8071966

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21.

P A Clark1, T Lester, L Villard, M Fontes, C Kinnon.   

Abstract

The three microsatellite repeat loci, DXS986, DXS995, and DXS1002, have been mapped to Xq13.2-21.1. We report here their relative order and their localisation within Xq21. These loci will be useful for the genetic mapping of disease loci in this region, in particular X linked deafness, as DXS995 lies in the region critical for this disorder.

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Year:  1994        PMID： 8071966      PMCID： PMC1049814          DOI： 10.1136/jmg.31.4.344

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


  11 in total

1.  A second-generation linkage map of the human genome.

Authors:  J Weissenbach; G Gyapay; C Dib; A Vignal; J Morissette; P Millasseau; G Vaysseix; M Lathrop
Journal:  Nature       Date:  1992-10-29       Impact factor: 49.962

2.  Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.

Authors:  I Bach; D Robinson; N Thomas; H H Ropers; F P Cremers
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

3.  Dinucleotide repeat polymorphism at the DXS441 locus.

Authors:  K T Ram; D F Barker; J M Puck
Journal:  Nucleic Acids Res       Date:  1992-03-25       Impact factor: 16.971

4.  Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.

Authors:  R G Lafrenière; C J Brown; V E Powers; L Carrel; K E Davies; D F Barker; H F Willard
Journal:  Genomics       Date:  1991-10       Impact factor: 5.736

5.  A simple, efficient method for the separate isolation of RNA and DNA from the same cells.

Authors:  N C Nicolaides; C J Stoeckert
Journal:  Biotechniques       Date:  1990-02       Impact factor: 1.993

6.  X-linked mental retardation: in pursuit of a gene map.

Authors:  C E Schwartz
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

7.  X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.

Authors:  J M Puck; R L Nussbaum; D L Smead; M E Conley
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

8.  The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.

Authors:  J M Puck; S M Deschênes; J C Porter; A S Dutra; C J Brown; H F Willard; P S Henthorn
Journal:  Hum Mol Genet       Date:  1993-08       Impact factor: 6.150

9.  Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans.

Authors:  M Noguchi; H Yi; H M Rosenblatt; A H Filipovich; S Adelstein; W S Modi; O W McBride; W J Leonard
Journal:  Cell       Date:  1993-04-09       Impact factor: 41.582

10.  Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease.

Authors:  Z Tümer; J Chelly; N Tommerup; Y Ishikawa-Brush; T Tønnesen; A P Monaco; N Horn
Journal:  Hum Mol Genet       Date:  1992-10       Impact factor: 6.150
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  4 in total

1.  Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis.

Authors:  T Lester; M de Alwis; P A Clark; A M Jones; F Katz; R J Levinsky; C Kinnon
Journal:  J Med Genet       Date:  1994-09       Impact factor: 6.318

2.  Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindred.

Authors:  S A Forbes; M Richardson; L Brennan; A Arnason; A Bjornsson; L Campbell; G Moore; P Stanier
Journal:  Hum Genet       Date:  1995-03       Impact factor: 4.132

3.  Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families.

Authors:  M Bitner-Glindzicz; Y de Kok; D Summers; I Huber; F P Cremers; H H Ropers; W Reardon; M E Pembrey; S Malcolm
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

4.  Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysis.

Authors:  P A Clark; T Lester; S Genet; A M Jones; R Hendriks; R J Levinsky; C Kinnon
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132
  4 in total

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