Mosca-Boidron, A L <br/><br/>
What can we learn from old microdeletion syndromes using array-CGH screening?  [electronic resource] 

 -  Clinical genetics  Jul 2012 
 - 41-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2011.01747.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adolescent<br/>Adult<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22--genetics<br/>Chromosomes, Human, Pair 7--genetics<br/>Comparative Genomic Hybridization<br/>Genotype<br/>Humans<br/>Intellectual Disability--diagnosis<br/>Karyotype<br/>Phenotype