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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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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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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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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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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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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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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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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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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Autosomal dominant cornea plana: Clinical findings in a Cuban family and a review of the literature von Sigler-Villanueva, Aldo, Tahvanainen, Esa, Lindh, Sinikka, Dieguez-Lucena, Jose, Forsius, Henrik

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The new university eye clinic at Oulu, Finland von Forsius, H

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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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Haplotype and multipoint linkage analysis in Finnish choroideremia families von SANKILA, E.-M, LEHNER, T, ERIKSSON, A. W, FORSIUS, H, KARNA, J, PAGE, D, OTT, J, DE LA CHAPELLE, A

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The use of genealogist in the study of hereditary eye disorders in northern Finland

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Linkage relationships and gene order around the locus for X-linked retinoschisis von Alitalo, T, sius, H, Kaarnaa, J, Frants, R R, Eriksson, A W, Wood, S, Kruse, T A, de la Chapelle, A

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Pseudoinflammatory Fundus Dystrophy with Autosomal Recessive Inheritance von Forsius, Henrik R., Eriksson, Aldur W., Suvanto, Erkki A., Alanko, Hannu I.

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Autosomal recessive cornea plana. A clinical and genetic study of 78 cases in Finland von Forsius, Henrik, Damsten, Margareta, Eriksson, Aldur W., Fellman, Johan, Lindh, Sinikka, Tahvanainen, Esa

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