Skip to main content

. 1991 Mar 11;19(5):1159. doi: 10.1093/nar/19.5.1159

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

G Shutler ¹, S Leblond ¹, J Bailly ¹, AE MacKenzie ¹, C Tsilfidis ¹, RG Korneluk ^1,^a

PMCID: PMC333807 PMID: 1673555

Abstract

1159

Images in this article

Image
on p.1159

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]
Smeets H., Bachinski L., Coerwinkel M., Schepens J., Hoeijmakers J., van Duin M., Grzeschik K. H., Weber C. A., de Jong P., Siciliano M. J. A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes. Am J Hum Genet. 1990 Mar;46(3):492–501. [PMC free article] [PubMed] [Google Scholar]

ACTIONS

RESOURCES