Literature DB >> 1673551

A frequent HincII polymorphism identified by the human chromosome 19q13.3 probe pKEX0.8 (D19S118).

C Tsilfidis1, G Shutler, M Mahadevan, R G Korneluk.   

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Year:  1991        PMID： 1673551      PMCID： PMC333804          DOI： 10.1093/nar/19.5.1157-a

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


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  1 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
  1 in total
  1 in total

1.  An informative panel of somatic cell hybrids for physical mapping on human chromosome 19q.

Authors:  L L Bachinski; R Krahe; B F White; B Wieringa; D Shaw; R Korneluk; L H Thompson; K Johnson; M J Siciliano
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025
  1 in total

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