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Browsing by Author Kamp, J.M. van de

Full Text	Issue Date	Title	Author(s)
	2009	CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis.	Dijk, F.S. Van; Nesbitt, I.M.; Nikkels, P.G.J.; Dalton, A.; Bongers, E.M.H.F., et al
	2007	Congenital disorder of glycosylation type Ia presenting with hydrops fetalis.	Kamp, J.M. van de; Lefeber, D.J.; Ruijter, G.J.; Steggerda, S.J.; Hollander, N.S., et al
	2004	Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease.	Drenth, J.P.H.; Tahvanainen, E.; Morsche, R.H.M. te; Tahvanainen, P.; Kaariainen, H., et al