Molecular Genetic Risk Screening von Grody, Wayne W

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ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals von De Wachter, E, De Boeck, K, Sermet-Gaudelus, I, Simmonds, NJ, Munck, A, Naehrlich, L, Barben, J, Boyd, C, Veen, SJ, Carr, SB, Fajac, I, Farrell, PM, Girodon, E, Gonska, T, Grody, WW, Jain, M, Jung, A, Kerem, E, Raraigh, KS, van Koningsbruggen-Rietschel, S, Waller, MD, Southern, KW, Castellani, C

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Targeted massively parallel sequencing provides comprehensive genetic diagnosis for patients with disorders of sex development von Arboleda, VA, Lee, H, Sánchez, FJ, Délot, EC, Sandberg, DE, Grody, WW, Nelson, SF, Vilain, E

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ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals von De Wachter, E, De Boeck, K, Sermet-Gaudelus, I, Simmonds, NJ, Munck, A, Naehrlich, L, Barben, J, Boyd, C, Veen, SJ, Carr, SB, Fajac, I, Farrell, PM, Girodon, E, Gonska, T, Grody, WW, Jain, M, Jung, Andreas, Kerem, E, Raraigh, KS, van Koningsbruggen-Rietschel, S, Waller, MD, Southern, KW, Castellani, C

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Cystic fibrosis population carrier screening: Here at last—Are we ready? von Grody, Wayne W, Desnick, Robert J

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Arginases I and II: do their functions overlap? von Cederbaum, Stephen D, Yu, Hong, Grody, Wayne W, Kern, Rita M, Yoo, Paul, Iyer, Ramaswamy K

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Mouse Model for Human Arginase Deficiency von Iyer, Ramaswamy K., Yoo, Paul K., Kern, Rita M., Rozengurt, Nora, Tsoa, Rosemarie, O'Brien, William E., Yu, Hong, Grody, Wayne W., Cederbaum, Stephen D.

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Comparative properties of arginases von Jenkinson, Christopher P., Grody, Wayne W., Cederbaum, Stephen D.

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The M694V mutationinArmenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA von Ong, FS, Vakil, H, Xue, Y, Kuo, JZ, Shah, KH, Lee, RB, Bernstein, KE, Rimoin, DL, Getzug, T, Das, K, Deignan, JL, Rotter, JI, Grody, WW

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Quality control in molecular genetic testing von Dequeker, Elisabeth, Ramsden, Simon, Grody, Wayne W., Stenzel, Timothy T., Barton, David E.

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Cloning and Characterization of Human Agmatinase von Iyer, Ramaswamy K., Kim, Ho K., Tsoa, Rosemarie W., Grody, Wayne W., Cederbaum, Stephen D.

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An electrochemical detection scheme for identification of single nucleotide polymorphisms using hairpin-forming probes von Huang, Tony Jun, Liu, Minghsun, Knight, Linda D., Grody, Wayne W., Miller, Jeff F., Ho, Chih-Ming

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Widespread Expression of Arginase I in Mouse Tissues: Biochemical and Physiological Implications von Yu, Hong, Yoo, Paul K, Aguirre, Claudia C, Tsoa, Rosemarie W, Kern, Rita M, Grody, Wayne W, Cederbaum, Stephen D, Iyer, Ramaswamy K

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The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA von Ong, FS, Vakil, H, Xue, Y, Kuo, JZ, Shah, KH, Lee, RB, Bernstein, KE, Rimoin, DL, Getzug, T, Das, K, Deignan, JL, Rotter, JI, Grody, WW

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Expression of arginase isozymes in mouse brain von Yu, Hong, Iyer, Ramaswamy K., Kern, Rita M., Rodriguez, Williams I., Grody, Wayne W., Cederbaum, Stephen D.

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Immunohistochemical evaluation of K- ras, p53, and HER-2/ neu expression in hyperplastic, dysplastic, and carcinomatous lesions of the pancreas: Evidence for multistep carcinogenes... von Apple, Sophia K, Randolph Hecht, J, Lewin, David N, Jahromi, Soraya A, Grody, Wayne W, Nieberg, Roberta K

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Cloning and Characterization of the Human Type II Arginase Gene von Vockley, Joseph G., Jenkinson, Christopher P., Shukla, Hridayabiranjan, Kern, Rita M., Grody, Wayne W., Cederbaum, Stephen D.

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Quest for Controls in Molecular Genetics von Grody, Wayne W.

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Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation von Ogino, S, Wilson, R B, Grody, W W

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The human arginases and arginase deficiency von Iyer, R., Jenkinson, C. P., Vockley, J. G., Kern, R. M., Grody, W. W., Cederbaum, S.

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