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Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients.
Pál M, Nagy D, Neller A, Farkas K, Leprán-Török D, Nagy N, Füstös D, Nagy R, Németh A, Szilvássy J, Rovó L, Kiss JG, Széll M. Pál M, et al. Int J Mol Sci. 2023 Apr 17;24(8):7401. doi: 10.3390/ijms24087401. Int J Mol Sci. 2023. PMID: 37108562 Free PMC article.
[Diagnosis of MECP2 duplication in a child and prenatally].
Bokor BA, Török D, Horváth E, László Z, Pál M, Szűcs P, Széll M. Bokor BA, et al. Among authors: pal m. Orv Hetil. 2024 Jan 7;165(1):30-34. doi: 10.1556/650.2024.32956. Print 2024 Jan 7. Orv Hetil. 2024. PMID: 38189840 Hungarian.
Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease.
Nagy N, Pal M, Kun J, Galik B, Urban P, Medvecz M, Fabos B, Neller A, Abdolreza A, Danis J, Szabo V, Yang Z, Fenske S, Biel M, Gyenesei A, Adam E, Szell M. Nagy N, et al. Among authors: pal m. Int J Mol Sci. 2024 Jan 20;25(2):1271. doi: 10.3390/ijms25021271. Int J Mol Sci. 2024. PMID: 38279271 Free PMC article.
1,081 results