Search Results - Spanjers, J.M.

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  1. 1
    Experiences with intrapartum fetal monitoring in the Netherlands: A survey study

    Experiences with intrapartum fetal monitoring in the Netherlands: A survey study by Habraken, Vera, Spanjers, Merel J.M., van der Woude, Daisy A.A., Oei, S. Guid, van Laar, Judith O.E.H.

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  2. 2
    The error-resistant interactively consistent architecture (ERICA)

    The error-resistant interactively consistent architecture (ERICA) by van Driel, C.-J.L., Follon, R.J.B., Kohler, A.A.C., van Osch, R.P.M., Spanjers, J.M.

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  3. 3
    A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC)

    A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC) by Wevers, R. A., Rijk‐van Andel, J. F., Bräutigam, C., Geurtz, B., Heuvel, L. P. W. J., Steenbergen‐Spanjers, G. C. H., Smeitink, J. A. M., Hoffmann, G. F., Gabreëls, F. J. M.

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  4. 4
    Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonism

    Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonism by Swaans, R J, Rondot, P, Renier, W O, Van Den Heuvel, L P, Steenbergen-Spanjers, G C, Wevers, R A

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  5. 5
    Exon skipping in the sterol 27-hydroxylase gene leads to cerebrotendinous xanthomatosis

    Exon skipping in the sterol 27-hydroxylase gene leads to cerebrotendinous xanthomatosis by 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
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