检索结果 - Catsman-Berrevoet..., C

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  1. 1
    Angelman syndrome: AS phenotype correlated with specific EEG pattern may result in a high detection rate of mutations in the UBE3A gene

    Angelman syndrome: AS phenotype correlated with specific EEG pattern may result in a high detection rate of mutations in the UBE3A gene 由 LAAN, L, VAN DEN OUWELAND, A M W, BAKKER, P, HALLEY, D, CATSMAN-BERREVOET..., C

    出版 1999
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  2. 2
    Tumour type and size are high risk factors for the syndrome of "cerebellar" mutism and subsequent dysarthria

    Tumour type and size are high risk factors for the syndrome of "cerebellar" mutism and subsequent dysarthria 由 Catsman-Berrevoet..., C., Van Dongen, H. R, Mulder, P., y, G, Paquier, P., Lequin, M.

    出版 1999
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  3. 3
    A new simple enzyme assay for pre- and postnatal diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) and its variants

    A new simple enzyme assay for pre- and postnatal diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) and its variants 由 Voznyi, Y, Keulemans, J, Mancini, G, Catsman-Berrevoet..., C, Young, E, Winchester, B, Kleijer, W, van Diggelen, O P

    出版 1999
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  4. 4
    Position effect on PLP1 may cause a subset of Pelizaeus-Merzbacher disease symptoms

    Position effect on PLP1 may cause a subset of Pelizaeus-Merzbacher disease symptoms 由 Muncke, N, Wogatzky, B, Breuning, M, Sistermans, E, Endris, V, Ross, M, Vetrie, D, Catsman-Berrevoet..., C, Rappold, G

    出版 2004
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