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Comments and Opinion | 24 December 2014
It is time to take timing seriously in clinical genetics
- György Kosztolányi
European Journal of Human Genetics 23 , 1435–1437

Rights & permissionsfor article It is time to take timing seriously in clinical genetics . Opens in a new window.
Research | 1 January 1999
No latent chromosome damage in oxygen-exposed premature neonates
Journal of Human Genetics 44 , 40–42

Rights & permissionsfor article No latent chromosome damage in oxygen-exposed premature neonates . Opens in a new window.
Research | 16 December 2010
Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations
- Kinga Hadzsiev
- , Noemi Polgar
- , Judit Bene
- , Katalin Komlosi
- , Judit Karteszi
- , Katalin Hollody
- , Gyorgy Kosztolanyi
- , Alessandra Renieri
- & Bela Melegh
Journal of Human Genetics 56 , 183–187

Rights & permissionsfor article Analysis of Hungarian patients with Rett syndrome phenotype for <i>MECP2</i>, <i>CDKL5</i> and <i>FOXG1</i> gene mutations . Opens in a new window.
Research | 1 May 2006
A novel IL2RG mutation associated with maternal T lymphocyte engraftment in a patient with severe combined immunodeficiency
- Richard Kellermayer
- , Amy P. Hsu
- , József Stankovics
- , Péter Balogh
- , Kinga Hadzsiev
- , Ágnes Vojcek
- , László Maródi
- , Pál Kajtár
- , György Kosztolányi
- & Jennifer M. Puck
Journal of Human Genetics 51 , 495–497

Rights & permissionsfor article A novel <i>IL2RG</i> mutation associated with maternal T lymphocyte engraftment in a patient with severe combined immunodeficiency . Opens in a new window.
Comments and Opinion | 30 June 2010
The medical geneticist as expert in the transgenerational and developmental aspects of diseases
- György Kosztolányi
- & Jean-Jacques Cassiman
European Journal of Human Genetics 18 , 1075–1076

Rights & permissionsfor article The medical geneticist as expert in the transgenerational and developmental aspects of diseases . Opens in a new window.
1 November 2006
Influence of Genetic Polymorphisms on Bone Disease of Preterm Infants
- Simone Funke
- , Éva Morava
- , Márta Czakó
- , Gabriella Vida
- , Tibor Ertl
- & György Kosztolányi
Pediatric Research 60 , 607–612

Rights & permissionsfor article Influence of Genetic Polymorphisms on Bone Disease of Preterm Infants . Opens in a new window.
Research | 7 May 2003
Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion
- Judit Bene
- , Edit Nádasi
- , György Kosztolányi
- , Károly Méhes
- & Béla Melegh
European Journal of Human Genetics 11 , 375–379

Rights & permissionsfor article Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion . Opens in a new window.
Reviews | 25 April 2006
The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues
European Journal of Human Genetics 14 , 588–645

Rights & permissionsfor article The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues . Opens in a new window.

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