Literature DB >> 2575587

Isolation of a novel mildly repetitive DNA sequence that is predominantly located at the terminus of the short arm of chromosome 4 near the Huntington disease gene.

M R Altherr1, B Smith, M E MacDonald, L Hall, J J Wasmuth.   

Abstract

A novel mildly repetitive DNA sequence that is reiterated approximately 20 times in the human genome has been isolated and characterized. Most of the repeat units are localized very near the terminus of the short arm of chromosome 4 (4p) in the region known to contain the Huntington disease (HD) gene. A cloned probe that detects the repeated sequence reveals a restriction fragment length polymorphism that is close to and/or distal to the most distal genetic locus on 4p. This probe, therefore, provides a new genetic marker very close to and possibly flanking the HD gene. In addition, this probe should prove very useful for detailed physical mapping of the most distal region of 4p around the HD gene. The few (two or three) copies of this repeat not located near the terminus of 4p are located near the ends of two other chromosomes, 14 and 21.

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Year:  1989        PMID: 2575587     DOI: 10.1016/0888-7543(89)90026-8

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  5 in total

1.  A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype.

Authors:  L L Estabrooks; A N Lamb; H N Kirkman; N P Callanan; K W Rao
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

2.  A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).

Authors:  S T Winokur; B Schutte; B Weiffenbach; S S Washington; D McElligott; A Chakravarti; J H Wasmuth; M R Altherr
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

3.  A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat.

Authors:  W el-Rifai; J Leisti; M Kähkönen; A Pietarinen; M R Altherr; S Knuutila
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

4.  Human aldehyde dehydrogenase: chromosomal assignment of the gene for the isozyme that metabolizes gamma-aminobutyraldehyde.

Authors:  J D McPherson; J J Wasmuth; G Kurys; R Pietruszko
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

5.  Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4.

Authors:  M R Altherr; U Bengtsson; F F Elder; D H Ledbetter; J J Wasmuth; M E McDonald; J F Gusella; F Greenberg
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025

  5 in total

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