Literature DB >> 2216806

Dinucleotide repeat polymorphism at the D21S168 locus.

Z Guo1, V Sharma, D Patterson, M Litt.   

Abstract

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Year:  1990        PMID： 2216806      PMCID： PMC332377          DOI： 10.1093/nar/18.19.5924-a

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


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  2 in total

1.  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.  Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions.

Authors:  K Gardiner; M Horisberger; J Kraus; U Tantravahi; J Korenberg; V Rao; S Reddy; D Patterson
Journal:  EMBO J       Date:  1990-01       Impact factor: 11.598
  2 in total
  3 in total

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

Authors: 
Journal:  Nucleic Acids Res       Date:  1991-07-25       Impact factor: 16.971

2.  Genetic variation of microsatellite markers D1S117, D6S89, D11S35, APOC2, and D21S168 in the Spanish population.

Authors:  J J Fuentes; I Banchs; V Volpini; X Estivill
Journal:  Int J Legal Med       Date:  1993       Impact factor: 2.686

3.  Exclusion of two candidate pigment loci, c and b, part of chromosome 11p, and 33 random polymorphic markers as the locus for tyrosinase-positive oculocutaneous albinism.

Authors:  M A Colman; G Stevens; M Ramsay; B Kwon; T Jenkins
Journal:  Hum Genet       Date:  1993-01       Impact factor: 4.132
  3 in total

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