Human Cholesterol Side-Chain Cleavage Enzyme, P450scc: cDNA Cloning, Assignment of the Gene to Chromosome 15, and Expression in the Placenta von Chung, Bon-Chu, Matteson, Karla J., Voutilainen, Raimo, Mohandas, T. K., Miller, Walter L.

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Structure of a bovine gene for P-450c21 (steroid 21-hydroxylase) defines a novel cytochrome P-450 gene family von Chung, B, Matteson, K.J, Miller, W.L

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Detection of ΔF508 mutation of the cystic fibrosis gene by matrix-assisted laser desorption/ionization mass spectrometry von Ch'Ang, L.-Y., Schell, M., Ringelberg, C., Tang, K., Matteson, K. J., Allman, S. L., Chen, C. H.

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Maternal antibrain antibodies in autism von Zimmerman, Andrew W, Connors, Susan L, Matteson, Karla J, Lee, Li-Ching, Singer, Harvey S, Castaneda, Julian A, Pearce, David A

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P450XXI (Steroid 21-hydroxylase) Gene Deletions are not Found in Family Studies of Congenital Adrenal Hyperplasia von Matteson, Karla J., Phillips, John A., Miller, Walter L., Chung, Bon-Chu, Orlando, Pamela J., Frisch, Herwig, Ferrandez, Angel, Burr, Ian M.

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Comparison of clonal relatedness and antimicrobial susceptibility of fecal Escherichia coli from healthy dogs and their owners von Stenske, Katherine A, Bemis, David A, Gillespie, Barbara E, D'Souza, Doris H, Oliver, Stephen P, Draughon, Francis A, Matteson, Karla J, Bartges, Joseph W

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Use of a molecular genetic approach to diagnosing the fragile X genotype von Potter, Nicholas T., Lozzio, Carmen B., Anderson, Ilse J., Bowlin, Enid S., Matteson, Karla J.

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A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locus von MATTESON, K. J, OSTRER, H, CHAKRAVARTI, A, BUETOW, K. H, ÓBRIEN, W. E, BEAUDET, A. L, PHILLIPS, J. A

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HPLC analysis of amino acids in inborn errors of metabolism von Matteson, K J

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Prevalence of urovirulence genes cnf, hlyD, sfa/foc, and papGIII in fecal Escherichia coli from healthy dogs and their owners von Stenske, Katherine A, Bemis, David A, Gillespie, Barbara E, Oliver, Stephen P, Draughon, Francis A, Matteson, Karla J, Bartges, Joseph W

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P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia von MATTESON, K. J, PHILLIPS, J. A. III, MILLER, W. L, BON-CHU CHUNG, ORLANDO, P. J, FRISCH, H, FERRANDEZ, A, BURR, I. M

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Regional evaluation of DNA diagnostic laboratories von Matteson, K J, Barker, P E, Kaplan, G C, Mueller, O T, Ostrer, H, Phillips, 3rd, J A, Schwartz, C

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Laser desorption mass spectrometry for point mutation detection von Taranenko, N.I, Matteson, K.J, Chung, C.N, Zhu, Y.F, Chang, L.Y, Allman, S.L, Haff, L, Martin, S.A, Chen, C.H

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Establishment of Stably EBV-Transformed Cell Lines from Residual Clinical Blood Samples for Use in Performance Evaluation and Quality Assurance in Molecular Genetic Testing von Bernacki, Susan H., Stankovic, Ana K., Williams, Laurina O., Beck, Jeanne C., Herndon, James E., Snow-Bailey, Karen, Prior, Thomas W., Matteson, Karla J., Wasserman, Linda M., Cole, Eugene C., Stenzel, Timothy T.

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Genetically Characterized Positive Control Cell Lines Derived from Residual Clinical Blood Samples von Bernacki, Susan H, Beck, Jeanne C, Stankovic, Ana K, Williams, Laurina O, Amos, Jean, Snow-Bailey, Karen, Farkas, Daniel H, Friez, Michael J, Hantash, Feras M, Matteson, Karla J, Monaghan, Kristin G, Muralidharan, Kasinathan, Pratt, Victoria M, Prior, Thomas W, Richie, Kristy L, Levin, Barbara C, Rohlfs, Elizabeth M, Schaefer, Frederick V, Shrimpton, Antony E, Spector, Elaine B, Stolle, Catherine A, Strom, Charles M, Thibodeau, Stephen N, Cole, Eugene C, Goodman, Barbara K, Stenzel, Timothy T

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New Directions in Cytogenetic and Molecular Testing of the Neonate von Anderson, Ilse J., Matteson, Karla J.

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Bioelectronic sensor technology for detection of cystic fibrosis and hereditary hemochromatosis mutations von Bernacki, Susan H, Farkas, Daniel H, Shi, Wenmei, Chan, Vivian, Liu, Yenbou, Beck, Jeanne C, Bailey, Karen Snow, Pratt, Victoria M, Monaghan, Kristin G, Matteson, Karla J, Schaefer, Frederick V, Friez, Michael, Shrimpton, Antony E, Stenzel, Timothy T

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Cloning and characterization of the bovine gene for steroid 21-hydroxylase (P-450c21) von Chung, B C, Matteson, K J, Miller, W L

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Methemoglobin reductase: Inactivation and protection against inactivation during disc gel electrophoresis von Matteson, Karla J., Taketa, Fumito

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An Approach to the Molecular Biology of Congenital Adrenal Hyperplasia von CHUNG, BON-CHU, MATTESON, KARLA J., MORIN, JOHN E., MELLON, SYNTHIA H., MILLER, WALTER L.

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