Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophy von Helderman-van den Enden, ATJM, De Jong, R, Den Dunnen, JT, Houwing-Duistermaat, JJ, Kneppers, ALJ, Ginjaar, HB, Breuning, MH, Bakker, E

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Duplications in the DMD gene von White, S.J., Aartsma-Rus, A., Flanigan, K.M., Weiss, R.B., Kneppers, A.L.J., Lalic, T., Janson, A.A.M., Ginjaar, H.B., Breuning, M.H., den Dunnen, J.T.

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Diagnostic Notch3 sequence analysis in CADASIL: Three new mutations in Dutch patients von OBERSTEIN, S. A. J. L, FERRARI, M. D, BAKKER, E, VAN GESTEL, J, KNEPPERS, A. L. J, FRANTS, R. R, BREUNING, M. H, HAAN, J

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Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family von Ginjaar, I B, Kneppers, A L, v d Meulen, J D, Anderson, L V, Bremmer-Bout, M, van Deutekom, J C, Weegenaar, J, den Dunnen, J T, Bakker, E

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Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy von GINJAAR, H. B, VAN DER KOOI, A. J, JEANPIERRE, M, BOLHUIS, P. A, MOORMAN, A. F. M, DE VISSER, M, BAKKER, E, OMMEN, G. J. B. V, CEELIE, H, KNEPPERS, A. L. J, VAN MEEGEN, M, BARTH, P. G, BUSCH, H. F. M, WOKKE, J. H. J, ANDERSON, L. V. B, BÖNNEMANN, C. G

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The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol von van Essen, A J, Kneppers, A L, van der Hout, A H, Scheffer, H, Ginjaar, I B, ten Kate, L P, van Ommen, G J, Buys, C H, Bakker, E

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Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contractures von Helderman-van den Enden, A.T.J.M., Ginjaar, H.B., Kneppers, A.L.J., Bakker, E., Breuning, M.H., de Visser, M.

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Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence risk von PASSOS-BUENO, M. R, BAKKER, E, KNEPPERS, A. L. J, TAKATA, R. I, RAPAPORT, DEN DUNNEN, J. T, ZATZ, M, VAN OMMEN, G. J. B

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Familial Paget's disease in The Netherlands: Occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations von Eekhoff, E. W. M., Karperien, M., Houtsma, D., Zwinderman, A. H., Dragoiescu, C., Kneppers, A. L. J., Papapoulos, S. E.

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First-trimester prenatal diagnosis in twin pregnancies von Christiaens, G. C. M. L., Oosterwijk, J. C., Stigter, R. H., Deutz-Terlouw, P. P., Kneppers, A. L. J., Bakker, E.

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