Literature DB >> 2882484

Isolation of a polymorphic DNA sequence pJSB11 (D19S16) from the human chromosome 19cen-q13.2 region linked to the myotonic dystrophy (DM) gene.

J Schepens, H Smeets, T Hulsebos, H Brunner, B Wieringa.   

Abstract

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Year:  1987        PMID： 2882484      PMCID： PMC340932          DOI： 10.1093/nar/15.7.3192

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


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  1 in total

1.  Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosome.

Authors:  T Hulsebos; B Wieringa; R Hochstenbach; D Smeets; J Schepens; F Oerlemans; J Zimmer; H H Ropers
Journal:  Cytogenet Cell Genet       Date:  1986
  1 in total
  3 in total

1.  Diagnosis of susceptibility to malignant hyperthermia with flanking DNA markers.

Authors:  S J Healy; J J Heffron; M Lehane; D G Bradley; K Johnson; T V McCarthy
Journal:  BMJ       Date:  1991-11-16

2.  Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy.

Authors:  H J Smeets; H G Brunner; H H Ropers; B Wieringa
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

3.  The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy.

Authors:  A E MacKenzie; R G Korneluk; F Zorzato; J Fujii; M Phillips; D Iles; B Wieringa; S Leblond; J Bailly; H F Willard
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025
  3 in total

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