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    Abstract PO-202: Copy number variation (CNV) analysis identifies variants in 1p36 in African American and Caucasian hereditary prostate cancer cases

    Abstract PO-202: Copy number variation (CNV) analysis identifies variants in 1p36 in African American and Caucasian hereditary prostate cancer cases von Williams, Alan F., Termine, Kirsten W., Waldron, John, Sartor, Oliver, Bailey-Wilson, Joan, Mandal, Diptasri


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    Abstract 1452: Analyses of whole exome sequencing (WES) data of hereditary lung cancer families identify germline copy number variations (CNVs) in multiple genes

    Abstract 1452: Analyses of whole exome sequencing (WES) data of hereditary lung cancer families identify germline copy number variations (CNVs) in multiple genes von Waldron, John, Termine, Kirsten W., Musolf, Anthony M., de Andrade, Mariza, Gaba, Colette, Govindan, Ramaswamy, Yang, Ping, You, Ming, Jaeger, Ellen, Bencaz, Angelle F., Anderson, Marshall W., Schwartz, Ann G., Pinney, Susan M., Amos, Christopher I., Bailey-Wilson, Joan E., Mandal, Diptasri M.

    Veröffentlicht in Cancer research (Chicago, Ill.)

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