Qidwai, Kanwal <br/><br/>
Deletions of Xp provide evidence for the role of holocytochrome C-type synthase (HCCS) in congenital diaphragmatic hernia.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jun 2010 
 - 1588-90 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.33410  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, X--genetics<br/>Hernia, Diaphragmatic--genetics<br/>Hernias, Diaphragmatic, Congenital<br/>Humans<br/>Lyases--genetics<br/>Male