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dc.contributor.authorRomagno, Daniela
dc.date.accessioned2022-05-31T10:11:41Z
dc.date.available2022-05-31T10:11:41Z
dc.date.issued2002
dc.identifierONIX_20220531_8884530555_3
dc.identifier.issn2704-6060
dc.identifier.urihttps://library.oapen.org/handle/20.500.12657/54720
dc.languageItalian
dc.relation.ispartofseriesScuole di dottorato
dc.subject.otherMedicina
dc.subject.otherGenetica
dc.subject.otherDNA
dc.subject.otherOpen Access
dc.titleGeni TBX e patologia umana
dc.typebook
oapen.abstract.otherlanguageTBX 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.
oapen.identifier.doi10.36253/88-8453-055-5
oapen.relation.isPublishedBybf65d21a-78e5-4ba2-983a-dbfa90962870
oapen.relation.isbn8884530555
oapen.series.number1
oapen.pages82
oapen.place.publicationFirenze


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