Literature DB >> 1673555

An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3.

G Shutler1, S Leblond, J Bailly, A E MacKenzie, C Tsilfidis, R G Korneluk.   

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Year:  1991        PMID： 1673555      PMCID： PMC333807          DOI： 10.1093/nar/19.5.1159

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


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  2 in total

1.  Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy.

Authors:  G Shutler; A E MacKenzie; H Brunner; B Wieringa; P de Jong; F P Lohman; S Leblond; J Bailly; R G Korneluk
Journal:  Genomics       Date:  1991-03       Impact factor: 5.736

2.  A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes.

Authors:  H Smeets; L Bachinski; M Coerwinkel; J Schepens; J Hoeijmakers; M van Duin; K H Grzeschik; C A Weber; P de Jong; M J Siciliano
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025
  2 in total
  1 in total

1.  The 1.5-Mb region spanning the myotonic dystrophy locus shows uniform recombination frequency.

Authors:  G G Shutler; A E MacKenzie; R G Korneluk
Journal:  Am J Hum Genet       Date:  1994-01       Impact factor: 11.025
  1 in total

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