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Browsing by Author Buysse, K.

Full Text	Issue Date	Title	Author(s)
	2010	Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy.	Collie, A.M.; Landsverk, M.L.; Ruzzo, E.; Mefford, H.C.; Buysse, K., et al
	2010	Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies.	Mefford, H.C.; Muhle, H.; Ostertag, P.; Spiczak, S. von; Buysse, K., et al
	2010	Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene.	Buysse, K.; Vergult, S.; Mussche, S.; Ceuterick-de Groote, C.; Speleman, F., et al
	2009	The 12q14 microdeletion syndrome: additional patients and further evidence that HMGA2 is an important genetic determinant for human height.	Buysse, K.; Reardon, W.; Mehta, L.; Costa, T.; Fagerstrom, C., et al
	2008	Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.	Mefford, H.C.; Sharp, A.J.; Baker, C.; Itsara, A.; Jiang, Z., et al
	2008	Mapping of 5q35 chromosomal rearrangements within a genomically unstable region.	Buysse, K.; Crepel, A.; Menten, B.; Pattyn, F.; Antonacci, F., et al