Literature DB >> 8449035

Confirmation of 15q26.1 as the site of the FES protooncogene by fluorescence in situ hybridization.

S Mathew1, V V Murty, J German, R S Chaganti.   

Abstract

The FES oncogene was previously localized to human chromosome 15 by analysis of mouse x human somatic cell hybrids and to 15q26 by in situ hybridization of a radioactively labeled probe. In the present study, using fluorescence in situ hybridization, we have determined the precise map position of FES at 15q26.1.

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Year:  1993        PMID： 8449035     DOI： 10.1159/000133496

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


  2 in total

1.  Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1.

Authors:  J German; A M Roe; M F Leppert; N A Ellis
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-05       Impact factor: 11.205

2.  Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome.

Authors:  N A Ellis; A M Roe; J Kozloski; M Proytcheva; C Falk; J German
Journal:  Am J Hum Genet       Date:  1994-09       Impact factor: 11.025
  2 in total

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