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Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Tissue specific mosaicism of trisomy 9 in a patient with severe torsion scoliosisE Morava, M Czakó, M Aszmann, et al.Journal of Inherited Metabolic Disease|March 10, 2025
The Therapeutic Future for Congenital Disorders of GlycosylationI J J Muffels, T Kozicz, E O Perlstein, et al.Urology|August 30, 2003
Metabolic findings after colocystoplasty in childrenP Vajda, A B Pinter, F Harangi, et al.The Journal of Pediatrics|August 1, 1994
Carnitine-dependent changes of metabolic fuel consumption during long-term treatment with valproic acidB Melegh, M Pap, E Morava, et al.Orvosi Hetilap|September 28, 2000
[22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot]E Morava, G Masszi, M Czakó, et al.Central European Journal of Public Health|June 17, 2000
Health risk factors and mortality in Pécs City, Hungary in the 1990sE Morava, E Végh, I Bóna, et al.Orvosi Hetilap|August 3, 2001
[Vascular diseases, spina bifida and schizophrenia in a single family associated with the heterozygote mutation of the heat-sensitive variant of methylenetetrahydrofolate reductase]A Horváth, E Morava, G Tóth, et al.Molecular Genetics and Metabolism|March 19, 2013
Thrombotic complications in patients with PMM2-CDGM Linssen, M Mohamed, R A Wevers, et al.Orvosi Hetilap|January 23, 1999
[Molecular biologic screening test (PCR) for fragile X syndrome]E Kovács, E Morava, E Nádasi, et al.Balkan Journal of Medical Genetics : BJMG|January 17, 2020
Infantile Alexander Disease with Late Onset Infantile Spasms and HypsarrhythmiaJ Paprocka, B Rzepka-Migut, N Rzepka, et al.Pageof 9