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Correspondence on "Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype" by Zanoni et al.
Cueto-González AM, Fernández-Álvarez P, Palafoll IV, Lasa-Aranzasti A, Vendrell Bayona T, Tizzano EF. Cueto-González AM, et al. Among authors: vendrell bayona t. Genet Med. 2022 Mar;24(3):754-756. doi: 10.1016/j.gim.2021.11.007. Epub 2021 Dec 6. Genet Med. 2022. PMID: 34906509 Free article. No abstract available.
Hypogammaglobulinemia in a 12-year-old patient with Jacobsen syndrome.
Fernández-San José C, Martín-Nalda A, Vendrell Bayona T, Soler-Palacín P. Fernández-San José C, et al. Among authors: vendrell bayona t. J Paediatr Child Health. 2011 Jul;47(7):485-6. doi: 10.1111/j.1440-1754.2011.02136.x. J Paediatr Child Health. 2011. PMID: 21771150 No abstract available.