Characterization of the Ocular Phenotype of Duchenne and Becker Muscular Dystrophy von Sigesmund, Dayle A., Weleber, Richard G., Pillers, De-Ann M., Westall, Carol A., Panton, Carole M., Powell, Berkley R., Héon, Elise, Murphey, William H., Musarella, Maria A., Ray, Peter N.

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A Heterozygous Putative Null Mutation in ROM1 without a Mutation in Peripherin/RDS in a Family with Retinitis Pigmentosa von Sakuma, Hitoshi, Inana, George, Murakami, Akira, Yajima, Toshihiro, Weleber, Richard G., Murphey, William H., Gass, J.Donald M., Hotta, Yoshihiro, Hayakawa, Mutsuko, Fujiki, Keiko, Gao, Yong Qing, Danciger, Michael, Farber, Debora, Cideciyan, Artur V., Jacobson, Samuel G.

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Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3 von Musarella, M.A., Weleber, R.G., Murphey, W.H., Young, R.S.L., Anson-Cartwright, L., Mets, M., Kraft, S.P., Polemeno, R., Litt, M., Worton, R.G.

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Dystrophin expression in the human retina is required for normal function as defined by electroretinography von Pillers, De-Ann M, Bulman, Dennis E, Weleber, Richard G, Sigesmund, Dayle A, Musarella, Maria A, Powell, Berkley R, Murphey, William H, Westall, Carol, Panton, Carole, Becker, Laurence E, Worton, Ronald G, Ray, Peter N

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Molecular advances in retinitis pigmentosa von Weleber, R. G., Murphey, W. H.

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SELECTIVE MEDIUM FOR CARBOHYDRATE-UTILIZING TRANSDUCTANTS OF STAPHYLOCOCCUS AUREUS von Murphey, W H, Rosenblum, E D

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Genetic heterogeneity among blue-cone monochromats von NATHANS, J, MAUMENEE, I. H, TRABOULSI, E, KLINGAMAN, R, BECH-HANSEN, N. T, LAROCHE, G. R, PAGON, R. A, MURPHEY, W. H, WELEBER, R. G, ZRENNER, E, SADOWSKI, B, SHARPE, L. T, LEWIS, R. A, HANSEN, E, ROSENBERG, T, SCHWARTZ, M, HECKENLIVELY, J. R

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Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicism von Naylor, E W, Murphey, W H, Domoszlai, E I, Guthrie, R

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Malate dehydrogenases. 3. Alteration of catalytic properties during purification of Bacillus subtilis malate dehydrogenases von Murphey, W H, Kaplan, N O

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Mannitol catabolism by Staphylococcus aureus von Murphey, W.H., Rosenblum, E.D.

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Genetic Recombination by Transduction Between Mannitol-Negative Mutants of Staphylococcus aureus von Murphey, W. H., Rosenblum, E. D.

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Serum carnosinase deficiency concomitant with mental retardation von Murphey, W H, Lindmark, D G, Patchen, L I, Housler, M E, Harrod, E K, Mosovich, L

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Neonatal hypothyroidism detected by the Northwest Regional Screening Program von LaFranchi, S H, Murphey, W H, Foley, Jr, T P, Larsen, P R, Buist, N R

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Oxytetracycline microfluorescent comparison of orthodontic retraction into recent and healed extraction sites von Murphey, Willis Hull

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Maternal phenylketonuria von Buist, N R, Lis, E W, Tuerck, J M, Murphey, W H

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Malate dehydrogenases. II. Purification and properties of Bacillus subtilis, Bacillus stearothermophilus, and Escherichia coli malate dehydrogenases von Murphey, W H, Barnaby, C, Lin, F J, Kaplan, N O

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Malate dehydrogenases. I. A survey of molecular size measured by gel filtration von Murphey, W H, Kitto, G B, Everse, J, Kaplan, N

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Transient Neonatal Hypothyroidism Detected by Newborn Screening Program von LAFRANCHI, STEPHEN H., BUIST, NEIL R. M., MURPHEY, WILLIAM H., LARSEN, P. REED, FOLEY, THOMAS P.

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Screening for congenital hypothyroidism: Results of screening one million North American infants von Fisher, Delbert A., Dussault, Jean H., Foley, Thomas P., Klein, Alan H., LaFranchi, Stephen, Larsen, P. Reed, Mitchell, Marvin L., Murphey, William H., Walfish, Paul G.

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Obstructive airway disease associated with heterozygous alpha-1 antitrypsin deficiency von Johnson, Thomas F., Reisman, Robert E., Arbesman, Carl E., Mattar, Adel G., Murphey, Willam H.

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