Literature DB >> 2612208

A somatic cell hybrid mapping panel for regional assignment of human chromosome 13 DNA sequences.

J K Cowell1, C D Mitchell.   

Abstract

We have constructed somatic cell hybrids containing different overlapping deletions involving human chromosome 13. Cytogenetic characterisation of the breakpoints allowed division of the chromosome into six distinct regions. Molecular characterisation of these hybrids allowed regional assignment of anonymous DNA sequences, cDNAs, and isoenzyme variants and these hybrids should prove valuable in the analysis and isolation of genes and disease loci on chromosome 13.

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Year:  1989        PMID： 2612208     DOI： 10.1159/000132827

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


  6 in total

1.  Band-specific localization of the microsatellite at D13S71 by microdissection and enzymatic amplification.

Authors:  H Spielvogel; H C Hennies; U Claussen; S S Washington; A Chakravarti; A Reis
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

2.  RFLP for intron E of factor XI gene.

Authors:  M G Butler; A D Parsons
Journal:  Nucleic Acids Res       Date:  1990-09-11       Impact factor: 16.971

3.  Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13.

Authors:  R F Kooy; A Y Van der Veen; E Verlind; R H Houwen; H Scheffer; C H Buys
Journal:  Hum Genet       Date:  1993-06       Impact factor: 4.132

4.  A duplicated region is responsible for the poly(ADP-ribose) polymerase polymorphism, on chromosome 13, associated with a predisposition to cancer.

Authors:  D Lyn; B W Cherney; M Lalande; J R Berenson; A Lichtenstein; S Lupold; K G Bhatia; M Smulson
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

5.  The 13q- syndrome: the molecular definition of a critical deletion region in band 13q32.

Authors:  S Brown; J Russo; D Chitayat; D Warburton
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

6.  Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: a case report.

Authors:  Can Liao; Fang Fu; Liang Zhang
Journal:  J Med Case Rep       Date:  2011-03-11
  6 in total

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