Zhang, Litu <br/><br/>
Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development.  [electronic resource] 

 -  European journal of human genetics : EJHG  Aug 2009 
 - 1010-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2008.269  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Animals<br/>Brain--embryology<br/>Chromosomes, Human, Pair 5<br/>Chromosomes, Human, Pair 8<br/>Heart--embryology<br/>Heart Defects, Congenital--genetics<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Mice<br/>Myocardium--metabolism<br/>Proto-Oncogene Proteins--genetics<br/>RUNX1 Translocation Partner 1 Protein<br/>Transcription Factors--genetics<br/>Translocation, Genetic