The library will operate on a duty schedule between 22 December 2025 and 4 January 2026. During this period, it will be possible to upload publications, but all other services will be suspended.
Madar, L.,
Majoros, V.,
Szűcs, Z.,
Nagy, O.,
Babicz, T.,
Butz, H.,
Patócs, A.,
Balogh, I.,
Koczok, K.:
Double Heterozygosity for Rare Deleterious Variants in the BRCA1 and BRCA2 Genes in a Hungarian Patient with Breast Cancer.
Int. J. Mol. Sci. 24 (20), 1-7, (article identifier: 15334), 2023.
Nagy, O.,
Kárteszi, J.,
Elmont, B.,
Ujfalusi, A.:
Case Report: Expressive Speech Disorder in a Family as Hallmark of 7q31 Deletion Involving the FOXP2 Gene.
Front. Pediatr. 9, 1-8, (article identifier: 664548), 2021.
Zodanu, G. K. E.,
Oszlánczi, M.,
Havasi, K.,
Kalapos, A.,
Rácz, G.,
Katona, M.,
Ujfalusi, A.,
Nagy, O.,
Széll, M.,
Nagy, D.:
Systemic Screening for 22q11.2 Copy Number Variations in Hungarian Pediatric and Adult Patients With Congenital Heart Diseases Identified Rare Pathogenic Patterns in the Region.
Front. Genet. 12, 1-11, (article identifier: 635480), 2021.
Nagy, O.,
Kárteszi, J.,
Hartwig, M.,
Bertalan, R.,
Jávorszky, E.,
Erhardt, É.,
Patócs, A.,
Tornóczky, T.,
Balogh, I.,
Ujfalusi, A.:
The importance of the multiplex ligation-dependent probe amplification in the identification of a novel two-exon deletion of the NR5A1 gene in a patient with 46,XY differences of sex development.
Mol. Biol. Rep. 46 (5), 5595-5601, 2019.
