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Browsing by Author Vergult, S.

Full Text	Issue Date	Title	Author(s)
	2011	Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions.	Vergult, S.; Krgovic, D.; Loeys, B.L.; Lyonnet, S.; Lieden, A., 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