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Browsing by Author Czako, M.

Full Text	Issue Date	Title	Author(s)
	2012	Infant with MCA and severe cutis laxa due to a de novo duplication 11p of paternal origin.	Gardeitchik, T.; Leeuw, N. de; Nijtmans, L.G.; Jira, P.; Kozicz, T.L., et al
	2007	[Metabolic bone disease in premature infants and genetic polymorphisms]	Funke, S.; Morava, E.; Czako, M.; Vida, G.; Ertl, T., et al
	2006	Influence of genetic polymorphisms on bone disease of preterm infants.	Funke, S.; Morava, E.; Czako, M.; Vida, G.; Ertl, T., et al
	2006	Transient progeroid phenotype and lipodystrophy in mosaic polyploidy.	Karteszi, J.; Kosztolanyi, G.Y.; Czako, M.; Hadzsiev, K.; Morava, E.
	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	Partial craniosynostosis in a patient with deletion 22q11.	Karteszi, J.; Kress, W.; Szasz, M.; Czako, M.; Melegh, B., et al
	2004	Opitz "C" trigonocephaly-like syndrome in a patient with terminal deletion of 2p and partial duplication of 17q.	Czako, M.; Riegel, M.; Morava, E.; Bajnoczky, K.; Kosztolanyi, G.Y.
	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