Devriendt, K <br/><br/>
The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease.  [electronic resource] 

 -  European journal of pediatrics  Aug 1996 
 - 721 p.  digital 
<br/><br/> Publication Type: Comment; Letter 
<br/><br/><label>ISSN: </label>0340-6199 
<br/><br/><label>Standard No.: </label>10.1007/BF01957162  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22<br/>Female<br/>Heart Defects, Congenital--epidemiology<br/>Humans<br/>Incidence<br/>Male<br/>Prospective Studies