Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype

Por Szabo, Andras, Czako, Marta, Hadzsiev, Kinga, Duga, Balazs, Komlosi, Katalin, Melegh, Bela
Publicado no Mol Cytogenet (2015)

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)