Chatfield, Kathryn C <br/><br/>
Congenital heart disease in Cornelia de Lange syndrome: phenotype and genotype analysis.  [electronic resource] 

 -  American journal of medical genetics. Part A  Oct 2012 
 - 2499-505 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>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.35582  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cell Cycle Proteins--genetics<br/>Chondroitin Sulfate Proteoglycans--genetics<br/>Chromosomal Proteins, Non-Histone--genetics<br/>De Lange Syndrome--genetics<br/>Female<br/>Genetic Association Studies<br/>Genotype<br/>Heart Defects, Congenital--diagnosis<br/>Humans<br/>Male<br/>Mutation<br/>Phenotype<br/>Proteins--genetics<br/>Severity of Illness Index<br/>Structural Maintenance of Chromosome Protein 1