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Browsing by Author Majoor-Krakauer, D.

Full Text	Issue Date	Title	Author(s)
	2011	Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy	Christiaans, I.; Birnie, E.; Bonsel, G.J.; Mannens, M.M.A.M.; Michels, M., et al
	2011	Distress in partners of individuals diagnosed with or at high risk of developing tumors due to rare hereditary cancer syndromes	Lammens, C.R.; Bleiker, E.M.; Verhoef, S.; Ausems, M.G.; Majoor-Krakauer, D., et al
	2011	Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis	Laar, I.M. van de; Oldenburg, R.A.; Pals, G.; Roos-Hesselink, J.W.; Graaf, B.M. de, et al
	2011	Compliance with periodic surveillance for Von-Hippel-Lindau disease	Lammens, C.R.; Aaronson, N.K.; Hes, F.J.; Links, T.P.; Zonnenberg, B.A., et al
	2010	Psychosocial impact of Von Hippel-Lindau disease: levels and sources of distress.	Lammens, C.R.; Bleiker, E.M.; Verhoef, S.; Hes, F.J.; Ausems, M.G., et al
	1996	A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)	Hofstra, R.M.; Osinga, J.; Sindhunata, G.T.; Wu, Y.; Kamsteeg, E.J., et al