Literature DB >> 8449514

Optimization of microsatellite analysis for genetic mapping.

A E Hughes1.   

Abstract

A method for typing microsatellite polymorphisms is described. It involves amplification using the polymerase chain reaction with one primer 5' end-labeled with 32P. Alleles are separated by denaturing gel electrophoresis and detected by autoradiography. Standardized conditions allow accurate typing of almost all microsatellite polymorphisms, and results are usually obtained within 24 h.

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Year:  1993        PMID： 8449514     DOI： 10.1006/geno.1993.1083

Source DB:  PubMed          Journal:  Genomics        ISSN： 0888-7543            Impact factor:   5.736


  8 in total

1.  Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21.

Authors:  W Van Hul; W Balemans; E Van Hul; F G Dikkers; H Obee; R J Stokroos; P Hildering; F Vanhoenacker; G Van Camp; P J Willems
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

2.  Isolation of dinucleotide repeats from a pig chromosome 1-specific DNA library.

Authors:  D V Dear; J R Miller
Journal:  Mamm Genome       Date:  1994-10       Impact factor: 2.957

3.  Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21.

Authors:  W Balemans; J Van Den Ende; A Freire Paes-Alves; F G Dikkers; P J Willems; F Vanhoenacker; N de Almeida-Melo; C F Alves; C A Stratakis; S C Hill; W Van Hul
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

4.  A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

Authors:  K Verhoeven; G Van Camp; P J Govaerts; W Balemans; I Schatteman; M Verstreken; L Van Laer; R J Smith; M R Brown; P H Van de Heyning; T Somers; F E Offeciers; P J Willems
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

5.  Association of two loci on chromosome 2q with nodal osteoarthritis.

Authors:  G D Wright; A E Hughes; M Regan; M Doherty
Journal:  Ann Rheum Dis       Date:  1996-05       Impact factor: 19.103

6.  A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9.

Authors:  S M Leal; F Apaydin; C Barnwell; M Iber; T Kandogan; M Pfister; U Braendle; O Cura; M Schwalb; H P Zenner; E Vitale
Journal:  Eur J Hum Genet       Date:  1998 Jul-Aug       Impact factor: 4.246

7.  Exclusion of the cartilage link protein and the cartilage matrix protein genes as the mutant loci in several heritable chondrodysplasias.

Authors:  J Loughlin; C Irven; B Sykes
Journal:  Hum Genet       Date:  1994-12       Impact factor: 4.132

8.  Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

Authors:  G Van Camp; M N Van Thienen; I Handig; B Van Roy; V S Rao; A Milunsky; A P Read; C T Baldwin; L A Farrer; M Bonduelle
Journal:  J Med Genet       Date:  1995-07       Impact factor: 6.318
  8 in total

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