Randomized Clinical Trial of Long-Acting Somatostatin for Autosomal Dominant Polycystic Kidney and Liver Disease by HOGAN, Marie C, MASYUK, Tetyana V, ROSSETTI, Sandro, HARRIS, Peter C, LARUSSO, Nicholas F, TORRES, Vicente E, PAGE, Linda J, KUBLY, Vickie J, BERGSTRALH, Eric J, XUJIAN LI, KIM, Bohyun, KING, Bernard F, GLOCKNER, James, HOLMES, David R

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Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3 by CONSUGAR, Mark B, KUBLY, Vickie J, LAGER, Donna J, HOMMERDING, Cynthia J, WAI CHONG WONG, BAKKER, Egbert, GATTONE, Vincent H, TORRES, Vicente E, BREUNING, Martijn H, HARRIS, Peter C

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Identification of Gene Mutations in Autosomal Dominant Polycystic Kidney Disease through Targeted Resequencing by ROSSETTI, Sandro, HOPP, Katharina, HARRIS, Peter C, SIKKINK, Robert A, SUNDSBAK, Jamie L, YEAN KIT LEE, KUBLY, Vickie, ECKLOFF, Bruce W, WARD, Christopher J, WINEARLS, Christopher G, TORRES, Vicente E

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The Frequency of Hereditary Defective Mismatch Repair in a Prospective Series of Unselected Colorectal Carcinomas by Cunningham, Julie M., Kim, Cheong-Yong, Christensen, Eric R., Tester, David J., Parc, Yann, Burgart, Lawrence J., Halling, Kevin C., McDonnell, Shannon K., Schaid, Daniel J., Walsh Vockley, Catherine, Kubly, Vickie, Nelson, Heidi, Michels, Virginia V., Thibodeau, Stephen N.

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Association of mutation position in polycystic kidney disease 1 ( PKD1) gene and development of a vascular phenotype by Rossetti, Sandro, Chauveau, Dominique, Kubly, Vickie, Slezak, Jeffrey M, Saggar-Malik, Anand K, Pei, York, Ong, Albert CM, Stewart, Fiona, Watson, Michael L, Bergstralh, Erik J, Winearls, Christopher G, Torres, Vicente E, Harris, Peter C

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