Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosis
Verrips, A., Lycklama à Nijeholt, G. J., Barkhof, F., Van Engelen, B. G. M., Wesseling, P., Luyten, J. A. F. M., Wevers, R. A., Stam, J., Wokke, J. H. J., van den Heuvel, L. P. W. J., Keyser, A., Gabreëls, F. J. M.
Published in Brain (London, England : 1878) (01.08.1999)
Published in Brain (London, England : 1878) (01.08.1999)
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Genetic characteristics of myoadenylate deaminase deficiency
Verzijl, H T, van Engelen, B G, Luyten, J A, Steenbergen, G C, van den Heuvel, L P, ter Laak, H J, Padberg, G W, Wevers, R A
Published in Annals of neurology (01.07.1998)
Published in Annals of neurology (01.07.1998)
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A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorder
JANSSEN, R. J. R. J., WEVERS, R. A., HÄUSSLER, M., LUYTEN, J. A. F. M., STEENBERGEN-SPANJERS, G. C. H., HOFFMANN, G. F., NAGATSU, T., VAN DEN HEUVEL, L. P. W. J.
Published in Annals of human genetics (01.09.2000)
Published in Annals of human genetics (01.09.2000)
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Conference Proceeding
Exon skipping in the sterol 27-hydroxylase gene leads to cerebrotendinous xanthomatosis
VERRIPS, A, STEENBERGEN-SPANJERS, G. C. H, LUYTEN, J. A. F. M, WEVERS, R. A, WOKKE, J. H. J, GABREËLS, F. J. M, WOLTHERS, B. G, VAN DEN HEUVEL, L. P. W. J
Published in Human genetics (01.08.1997)
Published in Human genetics (01.08.1997)
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Localization of the ICF Syndrome to Chromosome 20 by Homozygosity Mapping
Wijmenga, Cisca, van den Heuvel, Lambert P. W.J., Strengman, Eric, Luyten, Jan A.F.M., van der Burgt, Ineke J.A.M., de Groot, Ronald, Smeets, Dominique F.C.M., Draaisma, Jos M.T., van Dongen, Jacques J., De Abreu, Ronney A., Pearson, Peter L., Sandkuijl, Lodewijk A., Weemaes, Corry M.R.
Published in American journal of human genetics (01.09.1998)
Published in American journal of human genetics (01.09.1998)
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Verzijl, H. T. F. M., Van Engelen, B. G. M., Luyten, J. A. F. M., Steenbergen, G. C. H., Van Den Heuvel, L. P. W. J., Ter Laak, H. J., Padberg, G. W., Wevers, R. A.
Published in Annals of neurology (01.04.1999)
Published in Annals of neurology (01.04.1999)
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Verzijl, H. T. F. M., Van Engelen, B. G. M., Luyten, J. A. F. M., Steenbergen, G. C. H., Van Den Heuvel, L. P. W. J., Ter Laak, H. J., Padberg, G. W., Wevers, R. A.
Published in Annals of neurology (01.04.1999)
Published in Annals of neurology (01.04.1999)
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Verzijl, H. T. F. M., Van Engelen, B. G. M., Luyten, J. A. F. M., Steenbergen, G. C. H., Van Den Heuvel, L. P. W. J., Ter Laak, H. J., Padberg, G. W., Wevers, R. A.
Published in Annals of neurology (01.04.1999)
Published in Annals of neurology (01.04.1999)
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Metachromatic leukodystrophy: a 12-bp deletion in exon 2 of the arylsulfatase A gene in a late infantile variant
Luyten, J A, Wenink, P W, Steenbergen-Spanjers, G C, Wevers, R A, Ploos van Amstel, H K, de Jong, J G, van den Heuvel, L P
Published in Human genetics (01.09.1995)
Published in Human genetics (01.09.1995)
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