LEADER 03283nam 22008172 450 001 9910146163703321 005 20220812175939.0 010 $a88-8453-055-5 035 $a(CKB)1000000000280060 035 $a(ItFiC)it02717077 035 $a(MH)011326184-5 035 $a(SSID)ssj0000576840 035 $a(PQKBManifestationID)12187087 035 $a(PQKBTitleCode)TC0000576840 035 $a(PQKBWorkID)10558943 035 $a(PQKB)10471506 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/83697 035 $a(oapen)doab83697 035 $a(EXLCZ)991000000000280060 100 $a20050504d2002 uy 0 101 0 $aita 135 $aurmn|---annan 181 $ctxt 182 $cc 183 $acr 200 10$aGeni TBX e patologia umana /$fDaniela Romagno 210 $aFirenze $cFirenze university press$d2002 215 $a1 online resource (78 p.) 225 1 $aScuole di dottorato 225 0$aTesi: Scienze / Università degli studi di Firenze ;$v1 300 $aThesis. 320 $aIncludes bibliographical references. 330 $aTBX 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. 606 $aGenetics 606 $aPathology 606 $aCongenital, Hereditary, and Neonatal Diseases and Abnormalities 606 $aGenetic Phenomena 606 $aDNA-Binding Proteins 606 $aTranscription Factors 606 $aGenetic Phenomena 606 $aProteins 606 $aDisease 606 $aAmino Acids, Peptides, and Proteins 606 $aDrug Therapy 606 $aMutagenesis 606 $aT-Box Domain Proteins 606 $aCongenital Abnormalities 615 0$aGenetics. 615 0$aPathology. 615 2$aCongenital, Hereditary, and Neonatal Diseases and Abnormalities. 615 2$aGenetic Phenomena. 615 2$aDNA-Binding Proteins. 615 2$aTranscription Factors. 615 2$aGenetic Phenomena. 615 2$aProteins. 615 2$aDisease. 615 2$aAmino Acids, Peptides, and Proteins. 615 2$aDrug Therapy. 615 2$aMutagenesis. 615 2$aT-Box Domain Proteins. 615 2$aCongenital Abnormalities. 676 $a575 700 $aRomagno$b Daniela$01023055 801 0$bItFiC 801 1$bItFiC 801 2$bMH 906 $aBOOK 912 $a9910146163703321 996 $aGeni TBX e patologia umana$92430391 997 $aUNINA 999 $aThis Record contains information from the Harvard Library Bibliographic Dataset, which is provided by the Harvard Library under its Bibliographic Dataset Use Terms and includes data made available by, among others the Library of Congress