Voigt, R <br/><br/>
Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects.  [electronic resource] 

 -  Journal of medical genetics  Apr 2002 
 - e16 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.39.4.e16  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 10--genetics<br/>Chromosomes, Human, Pair 22--genetics<br/>Genetic Testing<br/>Heart Defects, Congenital--genetics<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Middle Aged<br/>Prospective Studies<br/>Syndrome