Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers von Hartmann, Lynn C., Sellers, Thomas A., Schaid, Daniel J., Frank, Thomas S., Soderberg, Cheryl L., Sitta, Diana L., Frost, Marlene H., Grant, Clive S., Donohue, John H., Woods, John E., McDonnell, Shannon K., Vockley, Catherine Walsh, Deffenbaugh, Amie, Couch, Fergus J., Jenkins, Robert B.

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The Frequency of Hereditary Defective Mismatch Repair in a Prospective Series of Unselected Colorectal Carcinomas von 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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Microsatellite instability in colorectal cancer : Different mutator phenotypes and the principal involvement of hMLH1 von THIBODEAU, S. N, FRENCH, A. J, FARR, G. H, O'CONNELL, M. J, CUNNINGHAM, J. M, TESTER, D, BURGART, L. J, ROCHE, P. C, MCDONNELL, S. K, SCHAID, D. J, VOCKLEY, C. W, MICHELS, V. V

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Detection of emerging HIV variants in blood donors from urban areas of Cameroon von LEE, S, WOOD, O, TANG, S, HU, J, MACHUCA, A, KERBY, S, AWAZI, B, VOCKLEY, C, HEWLETT, I

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Immunohistochemistry Versus Microsatellite Instability Testing in Phenotyping Colorectal Tumors von Lindor, N. M.

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Identification of 58 novel mutations in Niemann‐Pick disease type C: Correlation with biochemical phenotype and importance of PTC1‐like domains in NPC1 von Park, Walter D., O'Brien, John F., Lundquist, Patrick A., Kraft, Daniel L., Vockley, Cate Walsh, Karnes, Pamela S., Patterson, Marc C., Snow, Karen

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Counseling issues in genetic screening von Walsh-Vockley, C

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Introduction: new technologies for genetic and newborn screening von Seashore, M R, Walsh-Vockley, C

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The utility of brief questionnaire in assessment of risk for hereditary colorectal cancer in a clinic setting von TALAC, R, RABE, K, CUNNINGHAM, J, BOARDMAN, L, MICHELS, V, VOCKLEY, C, PETERSEN, G, THIBODEAU, S, NELSON, H

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p73 mutations are not detected in sporadic and hereditary breast cancer von SCHWARTZ, D. I, LINDOR, N. M, WALSH-VOCKLEY, C, ROCHE, P. C, MING MAI, SMITH, D. I, WANGUO LIU, COUCH, F. J

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Ultrastructure of an arterial lesion induced in rats by fenoldopam mesylate, a dopaminergic vasodilator von BUGELSKI, P. J, VOCKLEY, C. M. W, SOWINSKI, J. M, ARENA, E, BERKOWITZ, B. A, MORGAN, D. G

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A−2→G transition at the 3′ acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original stickler syndrome kindred von Williams, C. J., Ganguly, A., Considine, E., McCarron, S., Prockop, D. J., Walsh-Vockley, C., Michels, V. V.

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Genetic testing for Niemann-Pick Type C disease von Snow, K., Park, W.D., Lundquist, P.A., Vockley, C. Walsh, Patterson, M.C., Karnes, P.S., O’Brien, J.F.

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Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers von Hartmann, L C, Sellers, T A, Schaid, D J, Frank, T S, Soderberg, CL, Sitta, D L, Frost, M H, Grant, C S, Donohue, J H, Woods, JE, McDonnell, S K, Vockley, C W, Deffenbaugh, A, Couch, F J, Jenkins, R B

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Normal N-acetylglutamate concentration measured in liver from a new patient with N-acetylglutamate synthetase deficiency: Physiologic and biochemical implications von Vockley, Jerry, Vockley, Catherine M.Walsh, Lin, Shaun-Pei, Tuchman, Mendel, Wu, Tzee-Chung, Lin, Ching-Yuang, Seashore, Margretta R.

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Clustering gene expression time series data using an infinite Gaussian process mixture model von McDowell, Ian C, Manandhar, Dinesh, Vockley, Christopher M, Schmid, Amy K, Reddy, Timothy E, Engelhardt, Barbara E

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Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing von Bodian, Dale L, McCutcheon, Justine N, Kothiyal, Prachi, Huddleston, Kathi C, Iyer, Ramaswamy K, Vockley, Joseph G, Niederhuber, John E

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Mutations in NOTCH1 Cause Adams-Oliver Syndrome von Stittrich, Anna-Barbara, Lehman, Anna, Bodian, Dale L., Ashworth, Justin, Zong, Zheyuan, Li, Hong, Lam, Patricia, Khromykh, Alina, Iyer, Ramaswamy K., Vockley, Joseph G., Baveja, Rajiv, Silva, Ermelinda Santos, Dixon, Joanne, Leon, Eyby L., Solomon, Benjamin D., Glusman, Gustavo, Niederhuber, John E., Roach, Jared C., Patel, Millan S.

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Parent-of-origin-specific signatures of de novo mutations von Goldmann, Jakob M, Wong, Wendy S W, Pinelli, Michele, Farrah, Terry, Bodian, Dale, Stittrich, Anna B, Glusman, Gustavo, Vissers, Lisenka E L M, Hoischen, Alexander, Roach, Jared C, Vockley, Joseph G, Veltman, Joris A, Solomon, Benjamin D, Gilissen, Christian, Niederhuber, John E

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New observations on maternal age effect on germline de novo mutations von Wong, Wendy S. W., Solomon, Benjamin D., Bodian, Dale L., Kothiyal, Prachi, Eley, Greg, Huddleston, Kathi C., Baker, Robin, Thach, Dzung C., Iyer, Ramaswamy K., Vockley, Joseph G., Niederhuber, John E.

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