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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Clinical study of two brothers with a novel 33 bp duplication in the ARX gene von Demos, Michelle K., Fullston, Tod, Partington, Michael W., Gécz, Jozef, Gibson, William T.

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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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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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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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Clinical Sturdy of Two Brothers With a Novel 33 bp Ouplication in the ARX Gene von DEMOS, Michelle K, FULLSTON, Tod, PARTINGTON, Michael W, GECZ, Jozef, GIBSON, William T

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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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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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The Plasma Tyrosine Levels of Premature Babies von Mathews, John, Partington, Michael W.

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Reply von Turner, Gillian, Partington, Michael W

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Reply von Turner, Gillian, Partington, Michael W

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Reply von Turner, Gillian, Partington, Michael W

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Reply von Turner, Gillian, Partington, Michael W

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The plasma tyrosine levels of premature babies von MATTHEWS, JOHN, PARTINGTON, MICHAEL W

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Newborn screening for cystic fibrosis: Educational implications von Rae, John, Partington, Michael W.

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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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Cohen syndrome is neither uncommon nor new: Reply to Norio von Partington, Michael W., Anderson, Donald

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Clinical study of two brothers with a novel 33 bp duplication in the ARX gene von Demos, Michelle K., Fullston, Tod, Partington, Michael W., Gécz, Jozef, Gibson, William T.

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857 TWO UNUSUAL CASES OF β-GLUCURONIDASE DEFICIENCY (MPS VII) von Siegel, Jacqueline, Partington, Michael W, Clarke, Joe T R

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