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Browsing by Author Bakker, E.

Full Text	Issue Date	Title	Author(s)
	2012	The Muslim Brotherhood in Europe	Meijer, R.; Bakker, E.
	2011	Het einde van religieus terrorisme?: en wat daarna?	Lijn, J. van der; Bakker, E.
	2010	Becker muscular dystrophy patients with deletions around exon 51; a promising outlook for exon skipping therapy in Duchenne patients.	Helderman-van den Enden, A.T.; Straathof, C.S.; Aartsma-Rus, A.; Dunnen, J.T. den; Verbist, B.M., et al
	2009	Diplomatiek succes in Den Haag ook succes voor Afghanen? : kanttekeningen bij de Afghanistan-Conferentie	Lijn, J. van der; Bakker, E.
	2008	A novel (Leu183Pro-)mutation in the HFE-gene co-inherited with the Cys282Tyr mutation in two unrelated Dutch hemochromatosis patients.	Swinkels, D.W.; Venselaar, H.; Wiegerinck, E.T.G.; Bakker, E.; Joosten, I., 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
	2005	Towards the cloning of the H1 Gene	Goverse, A.; Bakker, E.; Tomczak, A.; Golas, T.M.; Achenbach, U., et al
	2004	Rusland werkt niet mee in de OVSE	Bakker, E.; Bomert, H.W.
	2004	Somatic mosaicism in FSHD often goes undetected.	Lemmers, R.J.L.F.; Wielen, M.J.R. van der; Bakker, E.; Padberg, G.W.A.M.; Frants, R.R., et al
	2004	Challenges for the OSCE - A Dutch perspective	Bakker, E.; Bomert, H.W.
	1997	BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients	Petrij-Bosch, A.; Peelen, T.; Vliet, M. van; Eijk, R. van; Olmer, R., et al
	1997	A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families	Peelen, T.; Vliet, M. van; Petrij-Bosch, A.; Mieremet, R.; Szabo, C., et al
	1997	More insight in the genetic mechanisms underlying facioscapulohumeral muscular dystrophy	Maarel, S.M. van der; Lemmers, R.J.L.; Deutekom, J.C.T. van; Bakker, E.; Wielen, M.J.R. van der, et al
	1997	Asymptomatic and late-onset ornithine transcarbamylase deficiency caused by a A208T mutation : Clinical, biochemical and DNA analyses in a four-generation family	Ausems, M.G.E.M.; Bakker, E.; Berger, R.A.; Duran, M.; Diggelen, O.P. van, et al
	1996	Asymptomatic and late-onset ornithine transcarbamylase (OTC) deficiency in males of a five-generation family, caused by an A208T mutation	Diggelen, O.P. van; Zaremba, J.; He, W.; Keulemans, J.L.M.; Boer, A.M., et al
	1996	Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: Diagnostic approach for sporadic and familial cases	Bakker, E.; Wielen, M.J.R. van der; Voorhoeve, E.; Ippel, P.F.; Padberg, G.W., et al
	1996	Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases	Bakker, E.; Wielen, M.J.R. van der; Voorhoeve, E.; Ippel, P.F.; Padberg, G.W.A.M., et al
	1996	Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26 : implications for genetic counselling and etiology of FSHD1	Deutekom, J.C.T. van; Bakker, E.; Lemmers, R.J.L.F.; Wielen, M.J.R. van der; Bik, E., et al
	1996	The clinical spectrum of limb girdle muscular dystrophy : a survey in the Netherlands	Kooi, A.J. van der; Barth, P.G.; Busch, H.F.M.; Haan, R.J. de; Ginjaar, H.B., et al
	1996	Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: Implications for genetic counselling and etiology of FSHD1	Deutekom, J.C.T. van; Bakker, E.; Lemmers, R.J.L.F.; Wielen, M.J.R. van der; Bik, E., et al
	1995	Early-Onset Facioscapulohumeral Muscular-Dystrophy	Brouwer, O.F.; Padberg, G.W.; Bakker, E.; Wijmenga, C.; Frants, R.R.
	1995	Facioscapulohumeral muscular dystrophy in the Dutch population	Padberg, G.W.A.M.; Frants, R.R.; Brouwer, O.F.; Wijmenga, C.; Bakker, E., et al
	1995	The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter	Bakker, E.; Wijmenga, C.; Vossen, R.H.A.M.; Padberg, G.W.A.M.; Hewitt, J.E., et al
	1995	Early onset facioscapulohumeral muscular dystrophy	Brouwer, O.F.; Padberg, G.W.A.M.; Bakker, E.; Wijmenga, C.; Frants, R.R.