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Dive into the research topics of 'Epitope-positive truncating MLH1 mutation and loss of PMS2: Implications for IHC-directed genetic testing for lynch syndrome'. Together they form a unique fingerprint.- Sort by
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Israel Zighelboim, Matthew A. Powell, Sheri A. Babb, Alison J. Whelan, Amy P. Schmidt, Mark Clendenning, Leigha Senter, Stephen N. Thibodeau, Albert De La Chapelle, Paul J. Goodfellow
Research output: Contribution to journal › Article › peer-review