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Browsing by Author Wijngaard, A. van de

Full Text	Issue Date	Title	Author(s)
	2007	Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.	Overeem, S.; Schelhaas, H.J.; Blijham, P.J.; Grootscholten, M.I.; Laak, H.J. ter, et al
	2006	Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation.	Verstraeten, V.L.; Broers, J.L.; Steensel, M.A.M. van; Zinn-Justin, S.; Ramaekers, F.C.S., et al
	1996	Genomic organization of the human bone morphogenetic protein-4 gene: molecular basis for multiple transcripts	Wijngaard, A. van de; Kraaij, M. van; Zoelen, E.J.J. van; Olijve, W.; Boersma, C.J.C.
	1995	Fine mapping of the human bone morphogenetic protein-4 gene (BMP4) to chromosome 14q22-q23 by in situ hybridization	Wijngaard, A. van de; Olde Weghuis, D.E.M.; Boersma, C.J.C.; Zoelen, E.J.J. van; Geurts van Kessel, A.H.M., et al
	1995	Fine mapping of the human bone morphogenetic protein-4 gene(BMP-4)to chromosome 14q22-q23 by in situ hybridization	Wijngaard, A. van de; Olde Weghuis, D.; Boersma, C.J.C.; Zoelen, E.J.J. van; Geurts van Kessel, A.H.M., et al