Functional analysis of the novel sequence variants within TBX5 gene promoter in patients with ventricular septal defects

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A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease

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Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

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Mortality in adult congenital heart disease

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Chromatin remodelling complex dosage modulates transcription factor function in heart development

Jun Takeuchi, Xin Lou, J M Alexander et al. · Nature Communications · 2011 · 212 citations · Full text

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