Etelka Postyeni

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

B. Melegh, K. Komlosi, K. Hadzsiev, 2016, Molecular Cytogenetics.

Whole Exome Sequencing in a Series of Patients with a Clinical Diagnosis of Tuberous Sclerosis Not Confirmed by Targeted TSC1/TSC2 Sequencing

A. Kelemen, B. Melegh, V. Farkas, 2021, Genes.

Age-Related Hearing Impairment Associated NAT2, GRM7, GRHL2 Susceptibility Gene Polymorphisms and Haplotypes in Roma and Hungarian Populations

J. Bene, B. Melegh, K. Komlosi, 2019, Pathology & Oncology Research.

Long-term Effects of the pituitary-adenylate cyclase-activating Polypeptide (PACAP38) in the Adult Mouse Retina: Microglial Activation and Induction of Neural Proliferation

R. Herczeg, R. Gábriel, Gergely Szarka, 2023, Neurochemical Research.