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Browsing by Author Mefford, H.C.

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
	2009	Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.	Bon, B.W.M. van; Mefford, H.C.; Menten, B.; Koolen, D.A.; Sharp, A.J., 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