Autosomal recessive Sorsby fundus dystrophy revisited : Molecular evidence for dominant inheritance von FELBOR, U, SUVANTO, E. A, FORSIUS, H. R, ERIKSSON, A. W, WEBER, B. H. F

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Abnormal crossing of the optic fibres shown by evoked magnetic fields in patients with ocular albinism with a novel mutation in the OA1 gene von Lauronen, L, Jalkanen, R, Huttunen, J, Carlsson, E, Tuupanen, S, Lindh, S, Forsius, H, Sankila, E-M, Alitalo, T

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Mutations in KERA , encoding keratocan, cause cornea plana von de la Chapelle, Albert, Joensuu, Tarja, Pellegata, Natalia S, Montgomery, Kate T, Lau, Stephanie, Krahe, Ralf, Kivelä, Tero, Dieguez-Lucena, Jose L, Forsius, Henrik, Kucherlapati, Raju

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Skewed secondary sex ratio in the offspring of carriers of the 214G > A mutation of the RS1 gene von HUOPANIEMI, L., FELLMAN, J., RANTALA, A., ERIKSSON, A., FORSIUS, H., DE LA CHAPELLE, A., ALITALO, T.

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The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study von Forsman, Eva, Lemmelä, Susanna, Varilo, Teppo, Kristo, Paula, Forsius, Henrik, Sankila, Eeva-Marja, Järvelä, Irma

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Linkage relationships and gene order around the locus for X-linked retinoschisis von ALITALO, T, FORSIUS, H, KARNA, J, FRANTS, R. R, ERIKSSON, A. W, WOOD, S, KRUSE, T. A, DE LA CHAPELLE, A

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Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in Finland von Huopaniemi, L, Rantala, A, Forsius, H, Somer, M, de la Chapelle, A, Alitalo, T

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Sex Ratio and Proportion of Affected Sons in Sibships with X-Chromosomal Recessive Traits: Maximum Likelihood Estimation in Truncated Multinomial Distributions von Fellman, Johan, Eriksson, Aldur W., Forsius, Henrik

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Autosomal Recessive Cornea Plana: In Vivo Corneal Morphology and Corneal Sensitivity von Vesaluoma, Minna H, Sankila, Eeva-Marja, Gallar, Juana, Muller, Linda J, Petroll, W. Matthew, Moilanen, Jukka A. O, Forsius, Henrik, Tervo, Timo M. T

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Dominantly and recessively inherited cornea plana congenita map to the same small region of chromosome 12 von Tahvanainen, E, Villanueva, A S, Forsius, H, Salo, P, de la Chapelle, A

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Changes of the eye caused by the climate in Rwanda, Africa von Forsius, Henrik, Maertens, Karel, Fellman, Johan

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The genetics of cornea plana congenita von Tahvanainen, E, Forsius, H, Kolehmainen, J, Damsten, M, Fellman, J, de la Chapelle, A

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Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis von Tahvanainen, Esa, Forsius, Henrik, Karila, Elvi, Ranta, Susanna, Eerola, Matti, Weissenbach, Jean, Sistonen, Pertti, de la Chapelle, Albert

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Tapeto-retinal degenerations with varying clinical features in Aland islanders von Forsius, H, Eriksson, A W

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Skewed secondary sex ratio in the offspring of carriers of the 214G > A mutation of the RS1 gene von Huopaniemi, L, Fellman, J, Rantala, A, Eriksson, A, sius, H, De La Chapelle, A, Alitalo, T

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Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis von Alitalo, T, Kruse, T A, Forsius, H, Eriksson, A W, de la Chapelle, A

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On Accidental Injuries to the Eyes in Finland von Forsius, H., Nikupaavo, A.

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X-LINKED HEREDITARY RETINOSCHISIS von Forsius, H., Vainio-Mattila, B., Eriksson, A.

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Linkage disequilibrium mapping of the cornea plana congenita gene CNA2 von TAHVANAINEN, E, FORSIUS, H, DAMSTEN, M, KARILA, E, KOLEHMAINEN, J, WEISSENBACH, J, SISTONEN, P, DE LA CHAPELLE, A

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Subacute sclerosing panencephalitis as a cause of chronic dementia and relapsing brain disorder von Donner, M., Waltimo, O., Porras, J., Forsius, H., Saukkonen, A.-L.

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