Search Results - Olderode-Berends, MJW

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  1. 1
    A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum

    A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum by Van Reeuwijk, J, Olderode-Berends, MJW, Van Den Elzen, C, Brouwer, OF, Roscioli, T, Van Pampus, MG, Scheffer, H, Brunner, HG, Van Bokhoven, H, Hol, FA

    Published in Clinical genetics
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  2. 2
    A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening

    A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening by Gerkes, E. H., Fock, J. M., den Dunnen, W. F. A., van Belzen, M. J., van der Lans, C. A., Hoving, E. W., Fakkert, I. E., Smith, M. J., Evans, D. G., Olderode-Berends, M. J. W.

    Published in Neurogenetics
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  3. 3
    Homozygous TMEM127 mutations in 2 patients with bilateral pheochromocytomas

    Homozygous TMEM127 mutations in 2 patients with bilateral pheochromocytomas by Eijkelenkamp, K., Olderode‐Berends, M.J.W., van der Luijt, R.B., Robledo, M., van Dooren, M., Feelders, R.A., de Vries, J., Kerstens, M.N., Links, T.P., van der Horst‐Schrivers, A.N.A.

    Published in Clinical genetics
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