Functional analysis of novel TBX5 T-box mutations associated with Holt–Oram syndrome
TBX3, TBX5, and the Ulnar-Mammary and Holt-Oram Syndromes
A New Mutation in the TBX5 Gene in Holt–Oram Syndrome: Two Cases in the Same Family and Prenatal Diagnosis
543miR-19a replacement rescues cardiac and fin defects in zebrafish model of holt-oram syndrome
Corrigendum to: Functional analysis of novel TBX5 T-box mutations associated with Holt–Oram syndrome
Characterization of the TBX5 binding site and analysis of mutations that cause Holt–Oram syndrome
Mayer–von Rokitansky–Küster–Hauser syndrome in association with a hitherto undescribed variant of the Holt–Oram syndrome with an aorto‐pulmonary window
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• The most common heart-hand syndrome.• Autosomal dominant.• Usually have an abnormal scaphoid with extra carpal bones.• Thumb is abnormal.• Get cardiac septal defects.
• The most common heart-hand syndrome.
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