Limb-girdle muscular dystrophy in the Netherlands : Gene defect identified in half the families von VAN DER KOOI, A. J, FRANKHUIZEN, W. S, BAKKER, E, GINJAAR, H. B, BARTH, P. G, HOWELER, C. J, PADBERG, G. W, SPAANS, F, WINTZEN, A. R, WOKKE, J. H. J, VAN OMMEN, G.-J. B, DE VISSER, M

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CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine von Stam, AH, Vanmolkot, KRJ, Kremer, HPH, Gärtner, J, Brown, J, Leshinsky-Silver, E, Gilad, R, Kors, EE, Frankhuizen, WS, Ginjaar, HB, Haan, J, Frants, RR, Ferrari, MD, Van Den Maagdenberg, AMJM, Terwindt, GM

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Risk of erroneous results in carrier testing for haemophilia A without prior DNA analysis in male index patients von Fransen van de Putte, D. E., Frankhuizen, W. S., Vijfhuizen, L., Groenewegen, L., Tamminga, R. Y. J., Bouman, K., van Essen, A. J., Gijsbers, A. C. J., Ruivenkamp, C. A. L., Boon, E. M. J.

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P2.47 Anoctamin 5 mutations in the Dutch limb girdle muscular dystrophy population von Frankhuizen, W.S, Verschuuren, J.J.G, van Doorn, P.A, de Visser, M, Ginjaar, H.B, van der Kooi, A.J

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Limb-girdle muscular dystrophy in the Netherlands: Gene defect identified in half the families von van der Kooi, AJ, Frankhuizen, W S, Barth, P G, Howeler, C J, Padberg, G W, Spaans, F, Wintzen, A R, Wokke, JHJ, van Ommen, G-JB, de Visser, M, Bakker, E, Ginjaar, H B

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Risk of erroneous results in carrier testing for haemophilia A without prior DNA analysis in male index patients von Fransen van de Putte, D E, Frankhuizen, W S, Vijfhuizen, L, Groenewegen, L, Tamminga, R Y J, Bouman, K, van Essen, A J, Gijsbers, A C J, Ruivenkamp, C A L, Boon, E M J

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Perspective of NIRS measurements early post mortem for prediction of pork quality von Hoving-Bolink, A.H., Vedder, H.W., Merks, J.W.M., de Klein, W.J.H., Reimert, H.G.M., Frankhuizen, R., van den Broek, W.H.A.M., Lambooij, en E.

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Prediction of pork quality attributes from near infrared reflectance spectra von Geesink, G.H, Schreutelkamp, F.H, Frankhuizen, R, Vedder, H.W, Faber, N.M, Kranen, R.W, Gerritzen, M.A

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P.182Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: the clinical and molecular spectrum of 244 patients von ten Dam, L., Frankhuizen, W., Linssen, W., Straathof, C., Niks, E., Faber, C., Fock, J., Kuks, J., Brusse, E., de Coo, I., Voermans, N., Verrips, A., Hoogendijk, J., van der Pol, W., Westra, D., de Visser, M., van der Kooi, A., Ginjaar, H.

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Butter and butter oil classification by PTR-MS von Ruth, S.M. van, Koot, A.H, Akkermans, W, Araghipour, N, Rozijn, M, Baltussen, M.A.H, Wisthaler, A, Mark, T.D, Frankhuizen, R

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Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display von HUANG, Yanchao, VERHEESEN, Peter, DE HAARD, Hans, BUSHBY, Kate, DEN DUNNEN, Johan, VAN DER MAAREL, Silvère M, ROUSSIS, Andreas, FRANKHUIZEN, Wendy, GINJAAR, Ieke, HALDANE, Faye, LAVAL, Steve, ANDERSON, Louise V. B, VERRIPS, Theo, FRANTS, Rune R

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Enzyme-linked immunosorbent assay for the detection of bovine rennet whey powder in milk powder and buttermilk powder von Bremer, Maria G.E.G., Kemmers-Voncken, Anna E.M., Boers, Eduard A.M., Frankhuizen, Rob, Haasnoot, Willem

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G.P.14.02 MLPA analysis of the CAPN3 gene detects large deletions in LGMD2A patients von Ginjaar, I, Tuit, S, Frankhuizen, W, van der Kooi, A, Doorn, P, Sival, D, Bakker, E

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