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. 1991 Mar 11;19(5):1158. doi: 10.1093/nar/19.5.1158-a

An SstI RFLP detected by the probe pKE2.1 (D19S116) localized to human chromosome 19q13.3

C Tsilfidis ¹, G Shutler ¹, S Leblond ¹, RG Korneluk ^1,^a

PMCID: PMC333806 PMID: 1673553

Abstract

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Shutler G., MacKenzie A. E., Brunner H., Wieringa B., de Jong P., Lohman F. P., Leblond S., Bailly J., Korneluk R. G. Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy. Genomics. 1991 Mar;9(3):500–504. doi: 10.1016/0888-7543(91)90416-c. [DOI] [PubMed] [Google Scholar]

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