Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel von Watson, Michael S., Cutting, Garry R., Desnick, Robert J., Driscoll, Deborah A., Klinger, Katherine, Mennuti, Michael, Palomaki, Glenn E., Popovich, Bradley W., Pratt, Victoria M., Rohlfs, Elizabeth M., Strom, Charles M., Richards, C. Sue, Witt, David R., Grody, Wayne W.

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Length of uninterrupted CGG repeats determines instability in the FMR1 gene von Reiss, Allan L, Thibodeau, Stephen N, Richards, C. Sue, Eichler, Evan E, Holden, Jeanette J.A, Popovich, Bradley W, Nelson, David L, Ward, Patricia A, Snow, Karen

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Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes von PARKS, Sharie B, POPOVICH, Bradley W, PRESS, Richard D

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Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophy von QUAN, F, JANAS, J, TOTH-FEJEL, S, JOHNSON, D. B, WOLFORD, J. K, POPOVICH, B. W

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Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation von BURMAN, R. W, POPOVICH, B. W, JACKY, P. B, TURKER, M. S

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A novel CAG repeat configuration in the SCA1 gene: implications for the molecular diagnostics of spinocerebellar ataxia type 1 von Quan, Franklin, Janas, Joanne, Popovich, Bradley W.

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Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism von Quan, Franklin, Grompe, Marcus, Jakobs, Petra, Popovich, Bradley W.

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Standards and Guidelines for CFTR Mutation Testing von Richards, Carolyn Sue, Bradley, Linda A., Amos, Jean, Allitto, Bernice, Grody, Wayne W., Maddalena, Anne, McGinnis, Matthew J., Prior, Thomas W., Popovich, Bradley W., Watson, Michael S.

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Hypomethylation of an Expanded FMR1 Allele Is Not Associated with a Global DNA Methylation Defect von Burman, Robert W., Yates, Phillip A., Green, Lindsay D., Jacky, Peter B., Turker, Mitchell S., Popovich, Bradley W.

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Cystic fibrosis carrier screening: Issues in implementation von Watson, Michael S., Desnick, Robert J., Grody, Wayne W., Mennuti, Michael T., Popovich, Bradley W., Richards, C Sue

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Advances for proficiency testing for genetic laboratory science von POPOVICH, Bradley W

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The impact of imprinting : Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunction von TOTH-FEJEL, S, OLSON, S, GUNTER, K, QUAN, F, WOLFORD, J, POPOVICH, B. W, MAGENIS, R. E

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Technical standards and guidelines: Venous thromboembolism (Factor V Leiden and prothrombin 20210G>A testing): A disease-specific supplement to the standards and guidelines for cli... von Spector, Elaine B., Grody, Wayne W., Matteson, Carla J., Palomaki, Glenn E., Bellissimo, Daniel B., Wolff, Daynna J., Bradley, Linda A., Prior, Thomas W., Feldman, Gerald, Popovich, Bradley W., Watson, Michael S., Richards, C Sue

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Effect of Ramadan Fasting on Moslem Kidney Transplant Recipients von Abdalla, Abdallah H., Shaheen, Faisal A., Rassoul, Zalmai, Owda, Ali K., Popovich, William F., Mousa, Dujanah H., Al-Hawas, Fahad, Al-Sulaiman, Mohammed H., Al-Khader, Abdullah A.

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A Small 55-Repeat MJD1 CAG Allele in a Patient with Machado-Joseph Disease and Abnormal Eye Movements von Egan, Robert A., Camicioli, Richard, Popovich, Bradley W.

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Correction of a Human βS-Globin Gene by Gene Targeting von Shesely, Edward G., Kim, Hyung-Suk, Shehee, W. Ronald, Papayannopoulou, Thalia, Smithies, Oliver, Popovich, Bradley W.

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Poultry Disease Risk Management: Biosecurity Instructional CD-ROM von Vaillancourt, Jean-Pierre, Lambert, Gene, Popovich, Laura W

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Use of i.v. iron saccharate in haemodialysis patients not responding to oral iron and erythropoietin von al-Hawas, F, Abdalla, A H, Popovich, W, Mousa, D H, al-Sulaiman, M H, al-Khader, A A

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Problems encountered in detecting a targeted gene by the polymerase chain reaction von Hyung-Suk, Kim, Popovich, Bradley W., Shehee, W.Ronald, Shesely, Edward G., Smithies, Oliver

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Molecular characterization of an atypical β-thalassemia caused by a large deletion in the 5'β-globin gene region von POPOVICH, B. W, ROSENBLATT, D. S, KENDALL, A. G, NISHIOKA, Y

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