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Browsing by Author Maat-Kievit, J.A.

Full Text	Issue Date	Title	Author(s)
	2011	Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations	Elfferich, P.; Verleun-Mooijman, M.C.T.; Maat-Kievit, J.A.; Warrenburg, B.P.C. van de; Abdo, W.F., et al
	2005	Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.	Bonifati, V.; Rohe, C.F.; Breedveld, G.J.; Fabrizio, E.; Mari, M. De, et al
	1995	Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardation	Maarel, S.M. van der; Scholten, I.H.J.M.; Maat-Kievit, J.A.; Huber, I.; Kok, Y.J.M. de, et al