TBX5 intragenic duplication: a family with an atypical Holt–Oram syndrome phenotype

Partial trisomy 12q: clinical and cytogenetic observations

(2010) C. Tengström et al.   CLINICAL GENETICS

A girl with severe expression of the Holt-Oram gene

(2010) R. J. M. Gardner et al.   CLINICAL GENETICS

Physical Interaction between TBX5 and MEF2C Is Required for Early Heart Development

(2009) T. K. Ghosh et al.   MOLECULAR AND CELLULAR BIOLOGY

Tbx4/5 gene duplication and the origin of vertebrate paired appendages

(2009) C. Minguillon et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome

(2008) Oleg A. Shchelochkov et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Functional analysis of the novel TBX5c.1333delC mutation resulting in an extended TBX5 protein

(2008) Johann Böhm et al.   BMC Medical Genetics

Atrial Fibrillation and Other Clinical Manifestations of Altered TBX5 Dosage in Typical Holt–Oram Syndrome

(2008) Deborah A. McDermott et al.   CIRCULATION RESEARCH

A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation

(2008) Alex V. Postma et al.   CIRCULATION RESEARCH

Conservation of linkage and evolution of developmental function within the Tbx2/3/4/5 subfamily of T-box genes: implications for the origin of vertebrate limbs

(2008) Amy C. Horton et al.   DEVELOPMENT GENES AND EVOLUTION