Tobias, E S <br/><br/>
Towards earlier diagnosis of 22q11 deletions.  [electronic resource] 

 -  Archives of disease in childhood  Dec 1999 
 - 513-4 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1468-2044 
<br/><br/><label>Standard No.: </label>10.1136/adc.81.6.513  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22<br/>Craniofacial Abnormalities--diagnosis<br/>DiGeorge Syndrome--genetics<br/>Heart Defects, Congenital--diagnosis<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Tetralogy of Fallot--genetics<br/>Time Factors