Literature DB >> 1762948

A sequence polymorphism in the human peripherin/RDS gene.

G J Farrar1, P Kenna, S A Jordan, R Kumar-Singh, P Humphries.   

Abstract

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Year:  1991        PMID： 1762948      PMCID： PMC329383          DOI： 10.1093/nar/19.24.6982-a

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


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  2 in total

1.  Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline----histidine substitution (codon 23) in pedigrees from Europe.

Authors:  G J Farrar; P Kenna; R Redmond; P McWilliam; D G Bradley; M M Humphries; E M Sharp; C F Inglehearn; R Bashir; M Jay
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

2.  The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA.

Authors:  G H Travis; L Christerson; P E Danielson; I Klisak; R S Sparkes; L B Hahn; T P Dryja; J G Sutcliffe
Journal:  Genomics       Date:  1991-07       Impact factor: 5.736
  2 in total
  2 in total

1.  Multiplex quantitative PCR using self-quenched primers labeled with a single fluorophore.

Authors:  Irina Nazarenko; Brian Lowe; Marlene Darfler; Pranvera Ikonomi; David Schuster; Ayoub Rashtchian
Journal:  Nucleic Acids Res       Date:  2002-05-01       Impact factor: 16.971

2.  A homogeneous, ligase-mediated DNA diagnostic test.

Authors:  X Chen; K J Livak; P Y Kwok
Journal:  Genome Res       Date:  1998-05       Impact factor: 9.043
  2 in total

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