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Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes.
Buerstedde, J M, Alday, P, Torhorst, J, Weber, W, Muller, H, Scott, RVolume:
32
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.32.11.909
Date:
November, 1995
File:
PDF, 643 KB
english, 1995