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Browsing by Author Korsch, E.

Full Text	Issue Date	Title	Author(s)
	2011	Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern	Mohamed, M.; Guillard, M.; Wortmann, S.B.; Cirak, S.; Marklova, E., et al
	2007	A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia.	Morava, E.; Zeevaert, R.; Korsch, E.; Huijben, K.M.; Wopereis, S., et al