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Browsing by Author Hadzsiev, K.

Full Text	Issue Date	Title	Author(s)
	2011	Mitochondrial dysfunction and organic aciduria in five patients carrying mutations in the Ras-MAPK pathway	Kleefstra, T.; Wortmann, S.B.; Rodenburg, R.J.T.; Bongers, M.H.F.; Hadzsiev, K., et al
	2008	Congenital disorder of glycosylation type Ix: review of clinical spectrum and diagnostic steps.	Morava, E.; Wosik, H.; Karteszi, J.; Guillard, M.; Adamowicz, M., et al
	2006	Transient progeroid phenotype and lipodystrophy in mosaic polyploidy.	Karteszi, J.; Kosztolanyi, G.Y.; Czako, M.; Hadzsiev, K.; Morava, E.
	2004	Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients.	Karteszi, J.; Hollody, K.; Bene, J.; Morava, E.; Hadzsiev, K., et al
	2004	[Mutational analysis of the MECP2 gene by direct sequencing in Hungarian patients with Rett syndrome]	Karteszi, J.; Hollody, K.; Bene, J.; Morava, E.; Hadzsiev, K., et al