Elliott, David A <br/><br/>
Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.  [electronic resource] 

 -  Journal of the American College of Cardiology  Jun 2003 
 - 2072-6 p.  digital 
<br/><br/> Publication Type: Comparative Study; Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0735-1097 
<br/><br/><label>Standard No.: </label>10.1016/s0735-1097(03)00420-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Australia<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Family Health<br/>Female<br/>Genes, Homeobox--genetics<br/>Genetic Markers--genetics<br/>Heart Block--genetics<br/>Heart Conduction System--pathology<br/>Heart Defects, Congenital--genetics<br/>Heart Septal Defects, Atrial--genetics<br/>Homeobox Protein Nkx-2.5<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Hypoplastic Left Heart Syndrome--genetics<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Middle Aged<br/>Point Mutation--genetics<br/>Polymorphism, Genetic--genetics<br/>Retrospective Studies<br/>Statistics as Topic<br/>Transcription Factors<br/>United States<br/>Xenopus Proteins