Localizaion of the gene for dominant cystoid macular dystrophy on chromosome 7p by Kremer, Hannie, Pinckers, Alfred, Helm, Bellinda van den, Deutman, August F., Ropers, Hans-HIlger, Mariman, Edwin C.M.

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A Novel Ribosomal S6-Kinase (RSK4; RPS6KA6) Is Commonly Deleted in Patients with Complex X-Linked Mental Retardation by Yntema, Helger G., van den Helm, Bellinda, Kissing, Johan, van Duijnhoven, Gerard, Poppelaars, Francis, Chelly, Jamel, Moraine, Claude, Fryns, Jean-Pierre, Hamel, Ben C.J., Heilbronner, Helmut, Pander, Hans-Jürgen, Brunner, Han G., Ropers, Hans-Hilger, Cremers, Frans P.M., van Bokhoven, Hans

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Localization of a Gene for Möbius Syndrome to Chromosome 3q by Linkage Analysis in a Dutch Family by Kremer, Hannie, Kuyt, Lambertus P., van den Helm, Bellinda, van Reen, Margo, Leunissen, Jack A. M., Hamel, Ben C. J., Jansen, Cees, Mariman, Edwin C. M., Frants, Rune R., Padberg, George W.

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Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family by DE BROUWER, Arjan P. M, PENNINGS, Ronald J. E, KIMBERLING, William J, CREMERS, Frans P. M, CREMERS, Cor W. R. J, KREMER, Hannie, ROETERS, Marjolijn, VAN HAUWE, Peter, ASTUTO, Lisa M, HOEFSLOOT, Lies H, HUYGEN, Patrick L. M, VAN DEN HELM, Bellinda, DEUTMAN, August F, BORK, Julie M

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Genetic heterogeneity of butterfly-shaped pigment dystrophy of the fovea by van Lith-Verhoeven, Janneke J C, Cremers, Frans P M, van den Helm, Bellinda, Hoyng, Carel B, Deutman, August F

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Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26 by Yntema, H G, Hamel, B C, Smits, A P, van Roosmalen, T, van den Helm, B, Kremer, H, Ropers, H H, Smeets, D F, van Bokhoven, H

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A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric region by Hamel, Ben C J, Wesseling, Pieter, Renier, Willy O, van den Helm, Bellinda, Ropers, Hans-Hilger, Kremer, Hannie, Mariman, Edwin C M

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X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3 by Siderius, Liesbeth E., Hamel, Ben C.J., van Bokhoven, Hans, de Jager, Frank, van den Helm, Bellinda, Kremer, Hannie, Heineman-de Boer, Josien A., Ropers, Hans-Hilger, Mariman, Edwin C.M.

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Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: Clinical and psychometric data and results of linkage analysis by Hamel, Ben C.J., Smits, Arie P.T., van den Helm, Bellinda, Smeets, Dominique F.C.M., Knoers, Nine V.A.M., van Roosmalen, Tanja, Thoonen, Geert H.J., Assman-Hulsmans, Claire F.C.H., Ropers, Hans-Hilger, Mariman, Edwin C.M., Kremer, Hannie

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X-linked mental retardation: Evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region by Yntema, Helger G., van den Helm, Bellinda, Knoers, Nine V.A.M., Smits, Arie P.T., van Roosmalen, Tanja, Smeets, Dominique F.C.M., Mariman, Edwin C.M., van der Burgt, Ineke, van Bokhoven, Hans, Ropers, Hans-Hilger, Kremer, Hannie, Hamel, Ben C.J.

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