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Browsing by Author Geurds, M.P.A.

Full Text	Issue Date	Title	Author(s)
	1996	PAX genes and human neural tube defects : an aminio acid substitution in PAX1 in a patient with spina bifida	Hol, F.A.; Geurds, M.P.A.; Chatkupt, S.; Shugart, Y.Y.; Balling, R., et al
	1995	Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family	Hol, F.A.; Hamel, B.C.J.; Geurds, M.P.A.; Hansmann, I.; Nabben, F.A.E., et al
	1995	A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome	Hol, F.A.; Hamel, B.C.J.; Geurds, M.P.A.; Mullaart, R.A.; Barr, F.G., et al
	1995	Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family	Hol, F.A.; Hamel, B.C.J.; Geurds, M.P.A.; Hansmann, I.; Nabben, F.A.E., et al
	1995	Absence of linkage between familial neural tube defects and PAX3 gene	Chatkupt, S.; Hol, F.A.; Shugart, Y.Y.; Geurds, M.P.A.; Stenroos, E.S., et al
	1995	A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome	Hol, F.A.; Hamel, B.C.J.; Geurds, M.P.A.; Mullaart, R.A.; Barr, F.G., et al
	1995	Production of native creatine kinase B in insect cells using a baculovirus expression vector	Kok, Y.J.M. de; Geurds, M.P.A.; Usmany, M.; Vlak, J.M.; Sistermans, E.A., et al