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Authors: Hargrave, M James, K Nield, K Toomes, C Georgas, K Sullivan, T Verzijl, HTFM Oley, CA Little, M De Jonghe, P Kwon, JM Kremer, H Dixon, MJ Tirnmerman, V Yamada, T Koopman, P
Citation: M. Hargrave et al., Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases, HUM GENET, 106(4), 2000, pp. 432-439

Authors: Verzijl, HTFM van Engelen, BGM Luyten, JAFM Steenbergen, GCH van den Heuvel, LPWJ ter Laak, HJ Padberg, GW Wevers, RA
Citation: Htfm. Verzijl et al., Primary, secondary, and coincidental types of myoadenylate deaminase deficiency - Reply, ANN NEUROL, 45(4), 1999, pp. 548-548

Authors: Verzijl, HTFM van den Helm, B Veldman, B Hamel, BCJ Kuyt, LP Padberg, GW Kremer, H
Citation: Htfm. Verzijl et al., A second gene for autosomal dominant Mobius syndrome is localized to chromosome 10q, in a Dutch family, AM J HU GEN, 65(3), 1999, pp. 752-756
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