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Browsing by Author Amor, D.J.

Full Text	Issue Date	Title	Author(s)
	2012	Dominant missense mutations in ABCC9 cause Cantu syndrome.	Harakalova, M.; Harssel, J.J. van; Terhal, P.A.; Lieshout, S. van; Duran, K., et al
	2010	Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes.	Bruno, D.L.; Anderlid, B.M.; Lindstrand, A.; Ravenswaaij-Arts, C.M.A. van; Ganesamoorthy, D., et al
	2009	Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.	Bijlsma, E.K.; Gijsbers, A.C.; Schuurs-Hoeijmakers, J.H.M.; Haeringen, A. van; Fransen van de Putte, D.E., et al