Literature DB >> 1891378

Dinucleotide repeat polymorphism at the D11S527 locus.

D L Browne1, J Gault, M B Thompson, X Y Hauge, G A Evans, M Litt.   

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Year:  1991        PMID： 1891378      PMCID： PMC328746          DOI： 10.1093/nar/19.17.4790-a

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


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  2 in total

1.  High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones.

Authors:  P Lichter; C J Tang; K Call; G Hermanson; G A Evans; D Housman; D C Ward
Journal:  Science       Date:  1990-01-05       Impact factor: 47.728

2.  Five polymorphic microsatellite VNTRs on the human X chromosome.

Authors:  J A Luty; Z Guo; H F Willard; D H Ledbetter; S Ledbetter; M Litt
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025
  2 in total
  8 in total

1.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1991-12-25       Impact factor: 16.971

2.  A partial hydatidiform mole with 2N/3N mosaicism identified by molecular analysis.

Authors:  Y Ikeda; Y Jinno; H Masuzaki; N Niikawa; T Ishimaru
Journal:  J Assist Reprod Genet       Date:  1996-10       Impact factor: 3.412

3.  Mapping eight new polymorphisms in 11q13 in the vicinity of multiple endocrine neoplasia type 1: identification of a new distal recombinant.

Authors:  C M Smith; S A Wells; D S Gerhard
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

4.  Linkage analysis in Usher syndrome type I (USH1) families from Spain.

Authors:  C Espinós; C Nájera; J M Millán; C Ayuso; M Baiget; H Pérez-Garrigues; O Rodrigo; C Vilela; M Beneyto
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

5.  Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q.

Authors:  E C Mariman; S E van Beersum; C W Cremers; F M van Baars; H H Ropers
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132

6.  Molecular evidence for non-penetrance in Best's disease.

Authors:  B H Weber; D Walker; B Müller
Journal:  J Med Genet       Date:  1994-05       Impact factor: 6.318

7.  The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533.

Authors:  Y Li; B Müller; C Fuhrmann; C E van Nouhuys; H Laqua; P Humphries; E Schwinger; A Gal
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

8.  Loss of heterozygosity at chromosome 11 in breast cancer: association of prognostic factors with genetic alterations.

Authors:  J Gudmundsson; R B Barkardottir; G Eiriksdottir; T Baldursson; A Arason; V Egilsson; S Ingvarsson
Journal:  Br J Cancer       Date:  1995-09       Impact factor: 7.640
  8 in total

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