Hypothesis: epigenetic effects will require a review of the genetics of child development

Por Kosztolányi, György
Publicado em 2011

It is time to take timing seriously in clinical genetics

Por Kosztolányi, György
Publicado no Eur J Hum Genet (2015)

3. Risk Assessment

Por Kosztolányi, György
Publicado no EJIFCC (2008)

The medical geneticist as expert in the transgenerational and developmental aspects of diseases

Por Kosztolányi, György, Cassiman, Jean-Jacques
Publicado em 2010

Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome

Por Komlósi, Katalin, Duga, Balázs, Hadzsiev, Kinga, Czakó, Márta, Kosztolányi, György, Fogarasi, András, Melegh, Béla
Publicado no Mol Cytogenet (2015)

Deletion of 4q28.3-31.23 in the background of multiple malformations with pulmonary hypertension

Por Duga, Balazs, Czako, Marta, Komlosi, Katalin, Hadzsiev, Kinga, Torok, Katalin, Sumegi, Katalin, Kisfali, Peter, Kosztolanyi, Gyorgy, Melegh, Bela
Publicado em 2014

Kleefstra syndrome in Hungarian patients: additional symptoms besides the classic phenotype

Por Hadzsiev, Kinga, Komlosi, Katalin, Czako, Marta, Duga, Balazs, Szalai, Renata, Szabo, Andras, Postyeni, Etelka, Szabo, Titanilla, Kosztolanyi, Gyorgy, Melegh, Bela
Publicado no Mol Cytogenet (2016)