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Browsing by Author Albrecht, B.

Full Text	Issue Date	Title	Author(s)
	2011	The relationship between ADHD and key cognitive phenotypes is not mediated by shared familial effects with IQ	Wood, A.C.; Rijsdijk, F.; Johnson, K.A.; Andreou, P.; Albrecht, B., et al
	2010	MACS syndrome: A combined collagen and elastin disorder due to abnormal Golgi trafficking.	Albrecht, B.; Brouwer, A.P.M. de; Lefeber, D.J.; Cremer, K.; Hausser, I., et al
	2010	Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar Syndrome.	Iqbal, Z.; Cejudo-Martin, P.; Brouwer, A.; Zwaag, B. van der; Ruiz-Lozano, P., et al
	2010	Separation of cognitive impairments in attention-deficit/hyperactivity disorder into 2 familial factors.	Kuntsi, J.; Wood, A.C.; Rijsdijk, F.; Johnson, K.A.; Andreou, P., et al
	2008	Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome.	Schulz, A.L.; Albrecht, B.; Arici, C.; Burgt, I. van der; Buske, A., et al
	2005	Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations.	So, J.; Suckow, V.; Kijas, Z.; Kalscheuer, V.M.M.; Moser, B., et al