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Browsing by Author Brouwer, A.

Full Text	Issue Date	Title	Author(s)
	2011	Estrogenic and androgenic activities in total plasma measured with reporter-gene bioassays: relevant exposure measures for endocrine disruptors in epidemiologic studies?	Brouwers, M.M.; Besselink, H.; Bretveld, R.W.; Anzion, R.B.M.; Scheepers, P.T.J., et al
	2010	Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.	Vermeer, S.; Hoischen, A.; Meijer, R.P.; Gilissen, C.F.H.A.; Neveling, K., et al
	2010	IFRS Leerboek	Backhuijs, J.; Braam, G.J.M.; Brouwer, A.; Ende, H. van den; Feijter, J. de, et al
	2010	Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar Syndrome.	Iqbal, Z.; Cejudo-Martin, P.; Brouwer, A.; Zwaag, B. van der; Ruiz-Lozano, P., et al
	2008	Competing Claims on Natural Resources: What Role for Science?	Giller, K.E.; Leeuwis, C.; Andersson, J.A.; Andriesse, W.; Brouwer, A., et al
	2007	Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation.	Chen, W.; Jensen, L.R.; Gecz, J.; Fryns, J.P.; Moraine, C., et al
	2007	Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.	Kousoulidou, L.; Parkel, S.; Zilina, O.; Palta, P.; Puusepp, H., et al
	2005	Antitrombotische therapie na een myocardinfarct : argumenten voor acetylsalicylzuur én cumarinederivaten	Waskowsky, W.M.; Brouwer, A.; Verheugt, F.W.A.