Boogerd, Cornelis J J <br/><br/>
Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome.  [electronic resource] 

 -  Cardiovascular research  Oct 2010 
 - 130-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1755-3245 
<br/><br/><label>Standard No.: </label>10.1093/cvr/cvq178  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Amino Acid Sequence<br/>Animals<br/>Atrial Natriuretic Factor--genetics<br/>Binding Sites<br/>Case-Control Studies<br/>Cell Line<br/>DNA Mutational Analysis<br/>Electrophoretic Mobility Shift Assay<br/>Fibroblast Growth Factor 10--genetics<br/>GATA4 Transcription Factor--genetics<br/>Genotype<br/>Heart Defects, Congenital--genetics<br/>Heart Septal Defects, Atrial--genetics<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Immunoprecipitation<br/>Lower Extremity Deformities, Congenital--genetics<br/>Models, Molecular<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Phenotype<br/>Promoter Regions, Genetic<br/>Protein Binding<br/>Protein Conformation<br/>Rats<br/>Recombinant Fusion Proteins--metabolism<br/>T-Box Domain Proteins--chemistry<br/>Transfection<br/>Upper Extremity Deformities, Congenital--genetics