Search Results - Lemmink, H.H.

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  1. 1
    Survival in SMA type I: A prospective analysis of 34 consecutive cases

    Survival in SMA type I: A prospective analysis of 34 consecutive cases by Cobben, J.M, Lemmink, H.H, Snoeck, I, Barth, P.A, van der Lee, J.H, de Visser, M

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  2. 2
    Single glycine deletion in COL7A1 acting as glycine substitution in dystrophic epidermolysis bullosa

    Single glycine deletion in COL7A1 acting as glycine substitution in dystrophic epidermolysis bullosa by Baardman, R., Bremer, J., Diercks, G.F.H., Jan, S.Z., Lemmink, H.H., Bolling, M.C., Van den Akker, P.C.

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    N.P.2 04 Patients with spinal muscular atrophy (SMA) and healthy siblings sharing homozygous deletions of the SMN1 gene reveal an identical number of SMN2 gene copies but different SMN protein levels

    N.P.2 04 Patients with spinal muscular atrophy (SMA) and healthy siblings sharing homozygous deletions of the SMN1 gene reveal an identical number of SMN2 gene copies but different... by Lemmink, H.H., Vos, Y.J., Plaza de Menacho, I., Dijkhuis, J., Knoers, N.V.A.M., de Visser, M., Buys, C.H.C.M.

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  4. 4
    The COL4A4 gene in mutated in familial benign hematuria

    The COL4A4 gene in mutated in familial benign hematuria by van der Loop, F.T.L., Lemmink, H.H., Niellesen, W.N., Brunner, H.G., Monnens, L.A.H., Schröder, C.H., Smeets, H.J.M.

    Published in Matrix biology
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