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Browsing by Author Kant, S.

Full Text	Issue Date	Title	Author(s)
	2007	Clinical and molecular phenotype of Aicardi-Goutieres syndrome.	Rice, G.; Patrick, T.; Parmar, R.; Taylor, C.F.; Aeby, A., et al
	2005	MRI supported diagnosis and counselling in a family with a probably autosomal recessive form of pachygyria.	Scherjon, S.A.; Liauw, L.; Kant, S.
	2004	Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux.	Bartels, C.F.; Bukulmez, H.; Padayatti, P.; Rhee, D.K.; Ravenswaaij-Arts, C.M.A. van, et al
	2004	Genotype-phenotype correlation in patients suspected of having sotos syndrome.	Boer, L.M.; Kant, S.; Karperien, M.; Beers, L. van; Tjon, J., et al