AAAAAA

   
Results: 1-7 |
Results: 7
Mild errors of morphogenesis in malignancy: Macroscopic manifestation of genetic instability?
Authors: Mehes, K
Citation: K. Mehes, Mild errors of morphogenesis in malignancy: Macroscopic manifestation of genetic instability?, MED PED ONC, 34(2), 2000, pp. 111-112
No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation
Authors: Kotzot, D Lurie, IW Mehes, K Werder, E Schinzel, A
Citation: D. Kotzot et al., No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation, CLIN GENET, 58(3), 2000, pp. 177-180
No latent chromosome damage in oxygen-exposed premature neonates
Authors: Mehes, K Bajnoczky, K Adamovich, K Khezri, S Kosztolanyi, G
Citation: K. Mehes et al., No latent chromosome damage in oxygen-exposed premature neonates, J HUM GENET, 44(1), 1999, pp. 40-42
No chromosomal instability in offspring of survivors of childhood malignancy
Authors: Bajnoczky, K Khezri, S Kajtar, P Szucs, R Kosztolanyi, G Mehes, K
Citation: K. Bajnoczky et al., No chromosomal instability in offspring of survivors of childhood malignancy, CANC GENET, 109(1), 1999, pp. 79-80
Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population
Authors: Gyurus, P Molnar, J Melegh, B Toth, G Morava, E Kosztolanyi, G Mehes, K
Citation: P. Gyurus et al., Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population, AM J MED G, 87(3), 1999, pp. 245-250
Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy
Authors: Melegh, B Seress, L Bedekovics, T Kispal, G Sumegi, B Trombitas, K Mehes, K
Citation: B. Melegh et al., Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy, J INH MET D, 22(7), 1999, pp. 827-838
Homoplastic A12,753G mitochondrial DNA mutation in a Hungarian family
Authors: Kis, A Matolcsy, A Vecsei, L Kosztolanyi, G Mehes, K Melegh, B
Citation: A. Kis et al., Homoplastic A12,753G mitochondrial DNA mutation in a Hungarian family, ACT BIOL HU, 49(1), 1998, pp. 119-124
Risultati: 1-7 |