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• W2110353287 endingPage "44" @default.
• W2110353287 startingPage "37R" @default.
• W2110353287 abstract "The T-box gene family encodes a large family of transcription factors with more than 20 members identified in humans so far, and homologues in many other organisms. A number of human disorders have been linked to mutations in T-box genes, confirming their medical importance. They include Holt– Oram syndrome/TBX5, Ulnar-Mammary syndrome/TBX3, and more recently DiGeorge syndrome/TBX1, ACTH deficiency/TBX19 and cleft palate with ankyloglossia/TBX22. This review describes the key features of these disorders and the involvement of T-box genes in their phenotype." @default.
• W2110353287 created "2016-06-24" @default.
• W2110353287 creator A5059934830 @default.
• W2110353287 date "2003-04-02" @default.
• W2110353287 modified "2023-09-30" @default.
• W2110353287 title "T-box genes in human disorders" @default.
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• W2110353287 doi "https://doi.org/10.1093/hmg/ddg077" @default.
• W2110353287 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12668595" @default.
• W2110353287 hasPublicationYear "2003" @default.
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