  |
Items where Author is "Bajnóczky, Katalin"
Group by: Item Type | No Grouping Jump to: Article Number of items: 7. ArticleKosztolányi, G. and Bajnóczky, Katalin and Méhes, K. (1991) Balanced chromosome rearrangements and abnormal phenotype. ACTA PAEDIATRICA, 31 (4). pp. 397-402. Bajnóczky, Katalin and Gardó, S. (1991) Familial extra bisatellited microchromosome and Down syndrome. ACTA PAEDIATRICA, 31 (4). pp. 403-406. Bajnóczky, Katalin and Meggyessy, Veronika (1985) Coincidence of paternal 13pYq translocation and maternal increased 13p NOR activity in a child with arthrogryposis and other malformations. ACTA PAEDIATRICA, 26 (2). pp. 151-156. Méhes, K. and Pelz, L. and Kosztolányi, G. and Bajnóczky, Katalin and Meggyessy, Veronika and Uhlemann, Marlies (1984) Neonatal intensive care does not cause chromosome damage. ACTA PAEDIATRICA, 25 (3). pp. 271-274. Méhes, K. and Bajnóczky, Katalin (1982) Normal chromosomes in liveborn neonates weighing less than 1000g. ACTA PAEDIATRICA, 23 (1). pp. 41-44. Bajnóczky, Katalin and Meggyessy, Veronika and Méhes, K. (1980) Cytogenetic investigations in prednisolone-treated infants. ACTA PAEDIATRICA, 21 (2-3). pp. 139-143. Bajnóczky, Katalin and Méhes, K. (1979) Down syndrome with XO/XX mosaicism. ACTA PAEDIATRICA, 20 (2-3). pp. 237-239. |
