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            Geni TBX e patologia umana

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            Author(s)
            Romagno, Daniela
            Language
            Italian
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            Abstract
            TBX genes belong to a family of homeotic genes (t-boxes) for which it has been proved that gene mutations have serious consequences on the development. In particular, there is significant evidence to support the involvement of the TBX1 gene in DiGeorge / Velocardiofacial syndrome (DGS/VCFS) and it has been proved that the TBX3 and TBX5 genes are implicated, respectively, in UMS (Ulnar Mammary Syndhrome) and in Holt-Oram syndrome (HOS). The book collects information available in the literature up to October 2001 on human TBX genes. The review of the data allowed to come to interesting considerations and offers ideas for orienting further research.
            URI
            https://doab-dev.siscern.org/handle/20.500.12854/195090
            Keywords
            Medicina; Genetica; DNA; Open Access
            DOI
            10.36253/88-8453-055-5
            ISBN
            8884530555
            Publisher
            Firenze University Press
            Publisher website
            www.fupress.com/
            Publication date and place
            Firenze, 2002
            Series
            Scuole di dottorato,
            Pages
            82
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              This project received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 871069.

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