Literature DB >> 6308738

Isolation of DNA fragments from chromosome 13.

T P Dryja, G A Bruns, S H Orkin, D M Albert, P S Gerald.   

Abstract

A number of patients with retinoblastoma have a deletion of chromosome 13. Comparison of the deleted segments from different individuals reveals that all deletions involve chromosome band 13q14. This observation has lead to the hypothesis that in this region is a gene of genes important in the etiology of retinoblastoma. As a first step toward understanding those genes, the authors successfully isolated five DNA fragments from chromosome 13 using recombinant DNA techniques. The DNA fragments from chromosome 13 will be useful in identifying DNA polymorphic sites that are linked to the retinoblastoma locus tentatively assigned to 13q14. Such DNA polymorphisms will be important in the genetic counselling of families with retinoblastoma. These chromosome 13q14 fragments also may be useful in searching for microdeletions of 13q14.

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Year:  1983        PMID: 6308738     DOI: 10.1097/00006982-198300320-00010

Source DB:  PubMed          Journal:  Retina        ISSN: 0275-004X            Impact factor:   4.256


  3 in total

1.  The 35 kd pulmonary surfactant-associated protein is encoded on chromosome 10.

Authors:  G Bruns; H Stroh; G M Veldman; S A Latt; J Floros
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

2.  Chromosome 13 restriction fragment length polymorphisms.

Authors:  T P Dryja; J M Rapaport; R Weichselbaum; G A Bruns
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

3.  DXS26 (HU16) is located in Xq21.1.

Authors:  E M Sankila; G A Bruns; M Schwartz; E Nikoskelainen; E Niebuhr; S V Hodgson; A F Wright; A de la Chapelle
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

  3 in total

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