Literature DB >> 2896341

Polymorphisms revealed by random probe H2-10 [D13S26] which maps to chromosome 13q21-q22.

A M Bowcock1, J M Hebert, L L Cavalli-Sforza.   

Abstract

Mesh：

Year:  1988        PMID： 2896341      PMCID： PMC336426          DOI： 10.1093/nar/16.6.2745

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  2 in total

1.  Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma.

Authors:  M Lalande; T Donlon; R A Petersen; R Liberfarb; S Manter; S A Latt
Journal:  Cancer Genet Cytogenet       Date:  1986-10

2.  Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus.

Authors:  M Lalande; T P Dryja; R R Schreck; J Shipley; A Flint; S A Latt
Journal:  Cancer Genet Cytogenet       Date:  1984-12
  2 in total
  2 in total

1.  DNA-based presymptomatic diagnosis of Wilson disease.

Authors:  D Gaffney; J L Walker; J G O'Donnell; G S Fell; K F O'Neill; R H Park; R I Russell
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Eight closely linked loci place the Wilson disease locus within 13q14-q21.

Authors:  A M Bowcock; L A Farrer; J M Hebert; M Agger; I Sternlieb; I H Scheinberg; C H Buys; H Scheffer; M Frydman; T Chajek-Saul
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025
  2 in total

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