Article Versions Notes

Riza A-L, Alkhzouz C, Farcaș M, Pîrvu A, Miclea D, Mihuț G, Pleșea R-M, Ștefan D, Drodar M, Lazăr C, et al. Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene. Genes. 2023; 14(1):69. https://doi.org/10.3390/genes14010069

Riza, Anca-Lelia, Camelia Alkhzouz, Marius Farcaș, Andrei Pîrvu, Diana Miclea, Gheorghe Mihuț, Răzvan-Mihail Pleșea, Delia Ștefan, Mihaela Drodar, Călin Lazăr, and et al. 2023. "Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene" Genes 14, no. 1: 69. https://doi.org/10.3390/genes14010069

Riza, A.-L., Alkhzouz, C., Farcaș, M., Pîrvu, A., Miclea, D., Mihuț, G., Pleșea, R.-M., Ștefan, D., Drodar, M., Lazăr, C., on behalf of the HINT Study, on behalf of the FUSE Study, Ioana, M., & Popp, R. (2023). Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene. Genes, 14(1), 69. https://doi.org/10.3390/genes14010069