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. 1991 Mar 11;19(5):1157. doi: 10.1093/nar/19.5.1157

A three allele insertion polymorphism is identified by the human chromosome 19q13.3 probe pKBE0.8 (D19S119)

RG Korneluk ¹, C Tsilfidis ¹, G Shutler ¹, M Mahadevan ¹, J Bailly ¹, LC Surh ¹

PMCID: PMC333803 PMID: 1673552

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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