DSpace at RU >

Browsing by Author Karteszi, J.

Full Text	Issue Date	Title	Author(s)
	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	Partial craniosynostosis in a patient with deletion 22q11.	Karteszi, J.; Kress, W.; Szasz, M.; Czako, M.; Melegh, B., et al
	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
	2004	Screening for CDG type Ia in Joubert syndrome.	Morava, E.; Cser, B.; Karteszi, J.; Huijben, K.M.; Szonyi, L., et al