MacDonald, Simon T <br/><br/>
Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency.  [electronic resource] 

 -  Cardiovascular research  Aug 2008 
 - 448-57 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0008-6363 
<br/><br/><label>Standard No.: </label>10.1093/cvr/cvn101  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Glands--abnormalities<br/>Animals<br/>Body Patterning<br/>Gene Expression Regulation, Developmental<br/>Germ Layers--metabolism<br/>Gestational Age<br/>Heart--embryology<br/>Heart Defects, Congenital--embryology<br/>Heterozygote<br/>Homeodomain Proteins--genetics<br/>Magnetic Resonance Imaging<br/>Mesoderm--metabolism<br/>Mice<br/>Mice, Inbred C57BL<br/>Mice, Knockout<br/>Myocardium--metabolism<br/>Neural Crest--metabolism<br/>Organogenesis<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Recombination, Genetic<br/>Repressor Proteins--genetics<br/>Trans-Activators--deficiency<br/>Transcription Factors--genetics<br/>Homeobox Protein PITX2