Characterization of Irradiated Metal Waste from the Pyrometallurgical Treatment of Used EBR-II Fuel von Westphal, Brian R., Frank, S. M., McCartin, W. M., Cummings, D. G., Giglio, J. J., O’Holleran, T. P., Hahn, P. A., Yoo, T. S., Marsden, K. C., Bateman, K. J., Patterson, M. N.

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Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UK von Viner, R M, Teoh, Y, Williams, D M, Patterson, M N, Hughes, I A

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Further Studies on the Recycle of Pyroprocessed Uranium von Westphal, B. R., Price, J. C., Patterson, M. N.

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Phenotypic diversity in siblings with partial androgen insensitivity syndrome von Evans, B A J, Hughes, I A, Bevan, C L, Patterson, M N, Gregory, J W

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Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome von Batch, J. A., Williams, D. M., Davies, H. R., Brown, B. D., Evans, B. A. J., Hughes, I. A., Patterson, M. N.

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Functional Analysis of Six Androgen Receptor Mutations Identified in Patients with Partial Androgen Insensitivity Syndrome von Bevan, Charlotte L., Brown, Betty B., Davies, Helen R., Evans, Bronwen A. J., Hughes, Ieuan A., Patterson, Mark N.

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An E-box within the MHC IIB gene is bound by MyoD and is required for gene expression in fast muscle von Wheeler, Matthew T, Snyder, Emily C, Patterson, Melissa N, Swoap, Steven J

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Wide variation in androgen receptor dysfunction in complete androgen insensitivity syndrome von Bevan, Charlotte L., Hughes, Ieuan A., Patterson, Mark N.

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Mutations of the androgen receptor gene identified in perineal hypospadias von Batch, J A, Evans, B A, Hughes, I A, Patterson, M N

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Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities von Clarkson, P A, Davies, H R, Williams, D M, Chaudhary, R, Hughes, I A, Patterson, M N

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Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndrome von Batch, J A, Davies, H R, Evans, B A, Hughes, I A, Patterson, M N

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Androgen insensitivity with mental retardation: a contiguous gene syndrome? von Davies, H R, Hughes, I A, Savage, M O, Quigley, C A, Trifiro, M, Pinsky, L, Brown, T R, Patterson, M N

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Linear order of new and established DNA markers around the fragile site at Xq27.3 von Hirst, M.C., Roche, A., Flint, T.J., MacKinnon, R.N., Bassett, J.H.D., Nakahori, Y., Watson, J.E.V., Bell, M.V., Patterson, M.N., Boyd, Y., Thomas, N.S.T., Knight, S.J.L., Warren, S.T., Hors-Cayla, M., Schmidt, M., Sutherland, G.R., Davies, K.E.

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MASA syndrome: further clinical delineation and chromosomal localisation von WINTER, R. M, DAVIES, K. E, BELL, M. V, HUSON, S. M, PATTERSON, M. N

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Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28 von BELL, M. V, BLOOMFIELD, J, MCKINLEY, M, PATTERSON, M. N, DARLISON, M. G, BARNARD, E. A, DAVIES, K. E

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An analysis of wood-burning installations from an environmental aspect von Fels, M., Cooper, D.F., Patterson, M.N.

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Androgen insensitivity syndrome von Williams, D M, Patterson, M N, Hughes, I A

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Physical mapping of DXS134 close to the DXS52 locus von BELL, M. V, PATTERSON, M. N, DORKINS, H. R, DAVIES, K. E

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Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome von Patterson, M.N., Bell, M.V., Bloomfield, J., Flint, T., Dorkins, H., Thibodeau, S.N., Schaid, D., Bren, G., Schwartz, C.E., Wieringa, b., Ropers, H.-H., Callen, D.F., Sutherland, G., Froster-Iskenius, U., Vissing, H., Davies, K.E.

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The androgen receptor gene mutations database von Patterson, M N, Hughes, I A, Gottlieb, B, Pinsky, L

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