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Browsing by Author Green, A.

Full Text	Issue Date	Title	Author(s)
	2012	Executive committee working group women in astronomy	Maddison, S.; Primas, F.; Aerts, C.; Clayton, G.; Combes, F., et al
	2011	Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis	Feenstra, I.; Hanemaaijer, N.; Sikkema-Raddatz, B.; Yntema, H.G.; Dijkhuizen, T., et al
	2010	Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients.	Hoornaert, K.P.; Vereecke, I.; Dewinter, C.; Rosenberg, T.; Beemer, F.A., et al
	2010	The clearwater consensus: The estimation of metal hazard in fresh water	Diamond, M.L.; Gandhi, N.; Adams, W.J.; Atherton, J.; Bhavsar, S.P., et al
	2010	Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of Lynch syndrome patients.	Klift, H.M. van der; Tops, C.M.; Bik, E.C.; Boogaard, M.W.; Borgstein, A.M., et al
	2010	UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients.	Leeuw, N. de; Bulk, S.; Green, A.; Jaeckle-Santos, L.; Baker, L.A., et al
	2009	Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy.	Lugtenberg, D.; Kleefstra, T.; Oudakker, A.R.; Nillesen, W.M.; Yntema, H.G., et al
	2007	No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease	Sanchez-Juan, P.; Bishop, M.T.; Green, A.; Giannattasio, C.; Arias Vasquez, A., et al