A follow-up study of mortality, health conditions and associated disabilities of people with intellectual disabilities in a Swedish county von Gustavson, K.-H., Umb-Carlsson, Õ., Sonnander, K.

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Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes von Cossée, Mireille, Dürr, Alexandra, Schmitt, Michèle, Dahl, Niklas, Trouillas, Paul, Allinson, Patricia, Kostrzewa, Markus, Nivelon-Chevallier, Annie, Gustavson, Karl-Henrik, Kohlschütter, Alfried, Müller, Ulrich, Mandel, Jean-Louis, Brice, Alexis, Koenig, Michel, Cavalcanti, Francesca, Tammaro, Angela, De Michele, Giuseppe, Filla, Alessandro, Cocozza, Sergio, Labuda, Malgorzata, Montermini, Laura, Poirier, Josée, Pandolfo, Massimo

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Re-evaluation of the dysequilibrium syndrome von Melberg, A., Örlén, H., Raininko, R., Entesarian, M., Dahlqvist, J., Gustavson, K. H., Dahl, N.

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Mild intellectual disability in children in Lahore, Pakistan: Aetiology and risk factors von Yaqoob, M., Bashir, A., Zaman, S., Ferngren, H., Von Dobeln, U., Gustavson, K.-H.

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Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family von Lindholm Carlström, Eva, Halvardson, Jonatan, Etemadikhah, Mitra, Wetterberg, Lennart, Gustavson, Karl-Henrik, Feuk, Lars

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Prevalence and associated impairments of mild mental retardation in six- to ten-year old children in Pakistan: a prospective study von Bashir, A, Yaqoob, M, Ferngren, H, Gustavson, K-H, Rydelius, P-A, Ansari, T, Zaman, S

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Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium von HÖGLUND, P, SISTONEN, P, NORIO, R, HOLMBERG, C, DIMBERG, A, GUSTAVSON, K.-H, DE LA CHAPELLE, A, KERE, J

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The Sjögren-Larsson Syndrome gene is close to D17S805 as determined by linkage analysis and allelic association von Sillén, Anna, Gustavson, Karl-Henrik, Wadelius, Claes, Weissenbach, Jean, Jagell, Sten, Pigg, Maritta

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Risk factors for mortality in young children living under various socio-economic conditions in Lahore, Pakistan: with particular reference to inbreeding von Yaqoob, Muhammad, Cnattingius, Sven, Jalil, Fehmida, Zaman, Shakila, Iselius, Lennart, Gustavson, Karl-Henrik

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Linkage mapping of a severe X-linked mental retardation syndrome von MALMGREN, H, SUNDVALL, M, DAHL, N, GUSTAVSON, K.-H, ANNEREN, G, WADELIUS, C, STEEN-BONDESON, M.-L, PETTERSSON, U

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Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene von Steén-Bondeson, M.-L., Dahl, N., Tönnesen, T., Kleijer, W.J., Seidlitz, G., Gustavson, K.-H., Wilson, P.J., Morris, C.P., Hopwood, J.J., Pettersson, U.

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Multiple epiphyseal dysplasia von Dahlqvist, Johanna, Örlén, Hanna, Matsson, Hans, Dahl, Niklas, Lönnerholm, Torsten, Gustavson, Karl-Henrik

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Further evidence of genetic homogeneity in Sjögren-Larsson syndrome von PIGG, M, ANNTON-LAMPRECHT, I, BRAUN-QUENTIN, C, GUSTAVSON, K.-H, WADELIUS, C

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Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304) von DAHL, N, GOONEWARDENA, P, MALMGREN, H, GUSTAVSON, K.-H, HOLMGREN, G, SEEMANOVA, E, ANNEREN, G, FLOOD, A, PETTERSSON, U

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Autosomal dominant cerebellar ataxia deafness and narcolepsy von Melberg, Atle, Hetta, Jerker, Dahl, Niklas, Nennesmo, Inger, Bengtsson, Mats, Wibom, Rolf, Grant, Crawford, Gustavson, Karl Henrik, Lundberg, Per Olov

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Isolation of a DNA probe of potential use for diagnosis of the fragile-x syndrome von DAHL, N, HAMMARSTROM-HEEROMA, K, GOONEWARDENA, P, WADELIUS, C, GUSTAVSON, K.-H, HOLMGREN, G, VAN OMMEN, G. J. B, PETTERSSON, U

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Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene von Richards, F M, Maher, E R, Latif, F, Phipps, M E, Tory, K, Lush, M, Crossey, P A, Oostra, B, Enblad, P, Gustavson, K H

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Complex aetiology of an apparently Mendelian form of mental retardation von Beleza-Meireles, Ana, Kockum, Ingrid, Yuan, Qiu-Ping, Picelli, Simone, Wetterberg, Lennart, Gustavson, Karl-Henrik, Schalling, Martin

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Substitution of glutamic acid for glycine 589 in the triple-helical domain of type III procollagen (COL3A1) in a family with variable phenotype of the Ehlers–Danlos syndrome type I... von Madhatheri, Swama L., Tromp, Gerard, Gustavson, Karl-Henrik, Kulvanlemi, Helena

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Reduced Optimality as an Indicator of Developmental Status at 18 Months and School Achievement at 8 Years von Sonnander, K., Gustavson, K. -H.

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