Literature DB >> 1549505

Dinucleotide repeat polymorphism at the D19S191 locus.

D E Iles1, B Segers, P de Jong, J Alleman, B Wieringa.   

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Year:  1992        PMID： 1549505      PMCID： PMC312147     

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


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  4 in total

1.  The G1021A substitution in the RYR1 gene does not cosegregate with malignant hyperthermia susceptibility in a British pedigree.

Authors:  A M Adeokun; S P West; F R Ellis; P J Halsall; P M Hopkins; A M Foroughmand; D E Iles; R L Robinson; A D Stewart; J L Curran
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

2.  Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19.

Authors:  J L Weber; Z Wang; K Hansen; M Stephenson; C Kappel; S Salzman; P J Wilkie; B Keats; N C Dracopoli; B F Brandriff
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

3.  Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.

Authors:  M Männikkö; M Kestailä; C Holmberg; R Norio; M Ryynänen; A Olsen; L Peltonen; K Tryggvason
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

4.  Refined genetic localization for central core disease.

Authors:  J C Mulley; H M Kozman; H A Phillips; A K Gedeon; J A McCure; D E Iles; R G Gregg; K Hogan; F J Couch; D H MacLennan
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025
  4 in total

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