P095: Recontacting patients with a CHEK2 or ATM pathogenic variant for updated NCCN screening guidelines: Report from an NCI-designated cancer center von Neimeyer, Katie, Brown, Lauren, Ching, Sidney, Handford, Cynthia, Sjoding, Britta, Tatunay, Kevin, Dubard-Gault, Marianne

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Initiation of universal tumor screening for Lynch syndrome in colorectal cancer patients as a model for the implementation of genetic information into clinical oncology practice von Cohen, Stacey A., Laurino, Mercy, Bowen, Deborah J., Upton, Melissa P., Pritchard, Colin, Hisama, Fuki, Jarvik, Gail, Fichera, Alessandro, Sjoding, Britta, Bennett, Robin L., Naylor, Lorraine, Jacobson, Angela, Burke, Wylie, Grady, William M.

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Initiation of universal tumor screening for L ynch syndrome in colorectal cancer patients as a model for the implementation of genetic information into clinical oncology practice von Cohen, Stacey A., Laurino, Mercy, Bowen, Deborah J., Upton, Melissa P., Pritchard, Colin, Hisama, Fuki, Jarvik, Gail, Fichera, Alessandro, Sjoding, Britta, Bennett, Robin L., Naylor, Lorraine, Jacobson, Angela, Burke, Wylie, Grady, William M.

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