Three new families with X-linked mental retardation caused by the 428-451dup(24bp) mutation in ARX von Partington, MW, Turner, G, Boyle, J, Gécz, J

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Familial colloid cysts of the third ventricle von Partington, MW, Bookalil, AJ

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Restoring reproductive confidence in families with X-linked mental retardation by finding the causal mutation von Turner, G, Boyle, J, Partington, MW, Kerr, B, Raymond, FL, Gécz, J

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Fragile X syndrome without CCG amplification has an FMR1 deletion von Gedeon, A.K, Baker, E, Robinson, H, Partington, M.W, Gross, B, Manca, A, Korn, B, Poustka, A, Yu, S, Sutherland 1, G.R, Mulley, J.C

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PAK3 mutation in nonsyndromic X-linked mental retardation von Allen, Kristina M., Gleeson, Joseph G., Bagrodia, Shubha, Partington, Michael W., MacMillan, John C., Cerione, Richard A., Mulley, John C., Walsh, Christopher A.

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Translocations involving 4p16.3 in three families: deletion causing the Pitt-Rogers-Danks syndrome and duplication resulting in a new overgrowth syndrome von Partington, M W, Fagan, K, Soubjaki, V, Turner, G

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Further segregation analysis of the fragile X syndrome with special reference to transmitting males von SHERMAN, S. L, JACOBS, P. A, MORTON, N. E, FROSTER-ISKENIUS, U, HOWARD-PEEBLES, P. N, NIELSEN, K. B, PARTINGTON, M. W, SUTHERLAND, G. R, TURNER, G, WATSON, M

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Another dystonia von Partington, M W

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Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndrome von Rogers, C, Partington, MW, Turner, GM

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Construction of a High-Resolution Linkage Map for Xp22.1-p22.2 and Refinement of the Genetic Localization of the Coffin-Lowry Syndrome Gene von Biancalana, Valerie, Trivier, Elisabeth, Weber, Chantal, Weissenbach, Jean, Rowe, Peter S.N., O'Riordan, Jeffrey L.H., Partington, Michael W., Heyberger, Sandra, Oudet, Claudine, Hanauer, Andre

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Genes for intelligence on the X chromosome von Turner, G, Partington, M W

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Leprosy in England then von Partington, MichaelW

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Apnea and sudden unexpected death in infants with achondroplasia von Pauli, Richard M., Scott, Charles I., Wassman, E. Robert, Gilbert, Enid F., Leavitt, Lewis A., Ver Hoeve, James, Hall, Judith G., Partington, Michael W., Jones, Kenneth Lyons, Sommer, Annemarie, Feldman, William, Langer, Leonard O., Rimoin, David L., Hecht, Jacqueline T., Lebovitz, Ruth

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Haematometra in the Langer-Giedion syndrome von Partington, M W, Rae, J, Payne, M J

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PAK3 mutation in nonsyndromic X-linked mental retardation von Walsh, Christopher A, Allen, Kristina M, Gleeson, Joseph G, Bagrodia, Shubha, Partington, Michael W, MacMillan, John C, Cerione, Richard A, Mulley, John C

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X-linked cutaneous amyloidosis: Further clinical and pathological observations von Partington, M. W., Prentice, R. S. A., Opitz, John M., Reynolds, James F.

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Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3 von Mulligan, L M, Phillips, M A, Forster-Gibson, C J, Beckett, J, Partington, M W, Simpson, N E, Holden, J J, White, B N

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Rubinstein-Taybi syndrome: A follow-up study von Partington, M. W.

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Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28 von Adès, L. C., Gedeon, A. K., Wilson, M. J., Latham, M., Partington, M. W., Mulley, J. C., Nelson, J., Lui, K., Sillence, D. O.

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Additional evidence for fragile X activity in heterozygous carriers von UCHIDA, I. A, FREEMAN, V. C. P, JAMRO, H, PARTINGTON, M. W, SOLTAN, H. C

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