Literature DB >> 3714479

A four-allele RFLP identified by an anonymous single copy genomic clone at 13q21-13qter [HGM8 assignment no. D13S12].

H Scheffer, D Penninga, N Goor, P L Pearson, C H Buys.   

Abstract

Mesh：

Year:  1986        PMID： 3714479      PMCID： PMC339872          DOI： 10.1093/nar/14.10.4374

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


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  4 in total

1.  Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma.

Authors:  K H Buetow; J C Murray; J L Israel; W T London; M Smith; M Kew; V Blanquet; C Brechot; A Redeker; S Govindarajah
Journal:  Proc Natl Acad Sci U S A       Date:  1989-11       Impact factor: 11.205

2.  Close linkage of the Wilson's disease locus to D13S12 in the chromosomal region 13q21 and not to ESD in 13q14.

Authors:  R H Houwen; H Scheffer; G J te Meerman; P van der Vlies; C H Buys
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

3.  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

4.  Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene.

Authors:  H Scheffer; R H Houwen; G J Te Meerman; J Loessner; B Bachmann; E Kunert; E Verlind; C H Buys
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132
  4 in total

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