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Browsing by Author Wouters, C.H.
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| Full Text | Issue Date | Title | Author(s) | | 2009 | FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome. | Fonzo, A. Di; Dekker, M.C.J.; Montagna, P.; Baruzzi, A.; Yonova, E.H., et al |
| 2007 | A t(4;6)(q12;p23) translocation disrupts a membrane-associated O-acetyl transferase gene (MBOAT1) in a patient with a novel brachydactyly-syndactyly syndrome. | Dauwerse, J.G.; Vries, B. de; Wouters, C.H.; Bakker, E.; Rappold, G.A., et al |
| 1987 | Cell surface characteristics and DNA content of macrophages in murine bone marrow cultures : a study using simultaneous scanning electron microscopy and fluorescence microscopy | Wouters, C.H.; Gevel, J.S. van de; Meer, J.W.M. van der; Daems, W.Th.; Furth, R. van, et al |
Showing results 1 to 3 of 3
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