A microarray screen for novel candidate genes in coeliac disease pathogenesis von Diosdado, B, Wapenaar, M C, Franke, L, Duran, K J, Goerres, M J, Hadithi, M, Crusius, J B A, Meijer, J W R, Duggan, D J, Mulder, C J J, Holstege, F C P, Wijmenga, C

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Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis von Wapenaar, M C, Monsuur, A J, van Bodegraven, A A, Weersma, R K, Bevova, M R, Linskens, R K, Howdle, P, Holmes, G, Mulder, C J, Dijkstra, G, van Heel, D A, Wijmenga, C

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Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications von DEN DUNNEN, J. T, GROOTSCHOLTEN, P. M, BAKKER, E, BLONDEN, L. A. J, GINJAAR, H. B, WAPENAAR, M. C, VAN PAASSEN, H. M. B, VAN BROECKHOVEN, C, PEARSON, P. L, VAN OMMEN, G. J. B

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Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil α-helical domains von DE CONCILIIS, L, MARCHITIELLO, A, BANFI, S, WAPENAAR, M. C, BORSANI, G, GIGLIO, S, MARIANI, M, CONSALEZ, G. G, ZUFFARDI, O, FRANCO, B, BALLABIO, A

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A gene from the Xp22.3 region shares homology with voltage-gated chloride channels von Slegtenhorst, Marjon A.van, T.Bassl, Maria, Borsanil, Gluseppe, Wapenaar, Martin C., Ferrero, Giovanni B., de Concillls, Lisa, Rugarli, Elena I., Grillo, Alessandra, Franco, Brunella, Y.Zoghbl, Huda, Ballabio, Andrea

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Association Analysis of MYO9B Gene Polymorphisms with Celiac Disease in a Swedish/Norwegian Cohort von Amundsen, Silja S., Monsuur, Alienke J., Wapenaar, Martin C., Lie, Benedicte A., Ek, Johan, Gudjónsdóttir, Audur H., Ascher, Henry, Wijmenga, Cisca, Sollid, Ludvig M.

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The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility von Wapenaar, Martin C., van Belzen, Martine J., Fransen, Justin H., Fariña Sarasqueta, Aranzazu, Houwen, Roderick H.J., Meijer, Jos W.R., Mulder, Chris J.J., Wijmenga, Cisca

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Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy von HOFKER, M. H, WAPENAAR, M. C, GOOR, N, BAKKER, E, VAN OMMEN, G.-J. B, PEARSON, P. L

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The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions von Wapenaar, Martin C., Bassl, Maria T., Schaefer, Laura, Grillo, Alessandra, Ferrero, Giovanni B., Chlnault, A.Craig, Ballabio, Andrea, Zoghbi, Huda Y.

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A Novel Splicing Mutation in KCNQ2 in a Multigenerational Family with BFNC Followed for 25 Years von De Haan, Gerrit‐Jan, Pinto, Dalila, Carton, Dietbrandt, Bader, Adri, Witte, Jorien, Peters, Edith, Van Erp, Gerard, Vandereyken, Willem, Boezeman, Eduard, Wapenaar, Martin C., Boon, Paul, Halley, Dicky, Koeleman, Bobby P. C., Lindhout, Dick

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Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect von Wijmenga, Cisca, Monsuur, Alienke J, Bakker, Paul I W de, Alizadeh, Behrooz Z, Zhernakova, Alexandra, Bevova, Marianna R, Strengman, Eric, Franke, Lude, Slot, Ruben van't, Belzen, Martine J van, Lavrijsen, Ineke C M, Diosdado, Begoña, Daly, Mark J, Mulder, Chris J J, Mearin, M Luisa, Meijer, Jos W R, Meijer, Gerrit A, Oort, Erica van, Wapenaar, Martin C, Koeleman, Bobby P C

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Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified... von Driesen, M.S., Dauwerse, J.G., Wapenaar, M.C., Meershoek, E.J., Mollevanger, P., Chen, K.L., Fischbeck, K.H., van Ommen, G.J.B.

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The X chromosome shows less genetic variation at restriction sites than the autosomes von HOFKER, M. H, SKRAASTAD, M. I, BERGEN, A. A. B, WAPENAAR, M. C, BAKKER, E, MILLINGTON-WARD, A, VAN OMMEN, G. J. B, PEARSON, P. L

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A CA-repeat polymorphism near DXS418 (P122) von De Vosse, E.Van, Booms, P.F.M., Vossen, R.H.A.M., Wapenaar, M.C., Ommen, G.J.B.Van, Dunnen, J.T.Den

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Physical mapping of 14 new DNA markers isolated from the human distal Xp region von Wapenaar, M.C., Petit, C., Basler, E., Ballabio, A., Henke, A., Rappold, G.A., van Paassen, H.M.B., Blonden, L.A.J., van Ommen, G.J.B.

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A high resolution deletion map of human chromosome Xp22 von Schaefer, Laura, Ferrero, Giovanni B, Grillo, Alessandra, Bassi, Maria T, Roth, Elizabeth J, Wapenaar, Martin C, van Ommen, Gert-Jan B, Mohandas, Thuluvancheri K, Rocchi, Mariano, Zoghbi, Huda Y, Ballabio, Andrea

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A submicroscopic deletion in a patient with isolated X-linked ocular albinism (OA1) von Bassi, Maria T., Bergen, Arthur A.B., Wapenaar, Martin C., Schlaffino, Maria V., van Schooneveld, Mary, Yates, John R.W., Charles, Stephen J., Meltinger, Thomas, Ballabio, Andrea

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P9 (DXYS75) detects a VNTR-type RFLP in the pseudoautosomal region von WAPENAAR, M. C, PEARSON, P. L, VAN OMMEN, G. J. B

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Deletion screening in patients with Duchenne muscular dystrophy von WULFF, K, HERRMANN, F. H, WAPENAAR, M. C, WEHNERT, M

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Isolation and Mapping of Human Chromosome 21 Cosmids Using a Probe for RTVL-H Retrovirus-like Elements von Meulenbelt, Ingrid, Wapenaar, Martin C., Patterson, David, Vijg, Jan, Uitterlinden, André G.

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