Jaillard, Sylvie <br/><br/>
Terminal 6.9 Mb deletion of chromosome 15q, associated with a structurally abnormal X chromosome in a patient with congenital diaphragmatic hernia and heart defect.  [electronic resource] 

 -  European journal of medical genetics   
 - 186-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2010.11.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Deletion<br/>Chromosome Inversion<br/>Chromosomes, Human, Pair 15<br/>Chromosomes, Human, X<br/>Female<br/>Heart Defects, Congenital--genetics<br/>Hernia, Diaphragmatic--genetics<br/>Hernias, Diaphragmatic, Congenital<br/>Humans<br/>Infant, Newborn<br/>X Chromosome Inactivation