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Browsing by Author Bruggenwirth, H.T.

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Full TextIssue DateTitleAuthor(s)
2012Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndrome.Laar, I.M. van de; Linde, D. van der; Oei, E.H.; Bos, P.K.; Bessems, J.H., et al
2010Mucopolysaccharidosis type IIIB may predominantly present with an attenuated clinical phenotype.Valstar, M.J.; Bruggenwirth, H.T.; Olmer, R.; Wevers, R.A.; Verheijen, F.W., et al
2010Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlations.Valstar, M.J.; Neijs, S.; Bruggenwirth, H.T.; Olmer, R.; Ruijter, G.J., et al
2006A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.Hout, A.H. van der; Ouweland, A.M.W. van den; Luijt, R.B. van der; Gille, H.J.; Bodmer, D., et al
2005Familial gigantism caused by an NSD1 mutation.Haelst, M.M. van; Hoogeboom, J.J.; Baujat, G.; Bruggenwirth, H.T.; Laar, I. van de, et al
Showing results 1 to 5 of 5

 

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