Items where authors include "Antanaviciute, A."

Article

Hany, U., Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (16 more authors) (2025) Genetic Screening of a Nonsyndromic Amelogenesis Imperfecta Patient Cohort Using a Custom smMIP Reagent for Selective Enrichment of Target Loci. Human Mutation, 2025. 8942542. ISSN 1059-7794

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. orcid.org/0009-0008-3593-8409 et al. (16 more authors) (2025) Genetic Screening of a nonsyndromic amelogenesis imperfecta patient cohort using a custom smMIP reagent for selective enrichment of target loci. Human Mutation, 2025 (1). 8942542. ISSN 1059-7794

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (17 more authors) (2024) Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta. Journal of Medical Genetics, 61 (4). pp. 347-355. ISSN 0022-2593

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (17 more authors) (2024) Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta. Journal of Medical Genetics, 61 (4). pp. 347-355. ISSN 0022-2593

Baquero-Perez, B., Antanaviciute, A., Yonchev, I.D. et al. (3 more authors) (2019) The tudor SND1 protein is an m6A RNA reader essential for replication of Kaposi’s sarcoma-associated herpesvirus. eLife, 8. 47261.