Brown, Natasha <br/><br/>
5q31.3 Microdeletion syndrome: clinical and molecular characterization of two further cases.  [electronic resource] 

 -  American journal of medical genetics. Part A  Oct 2013 
 - 2604-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.36108  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Brain--pathology<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 5<br/>Comparative Genomic Hybridization<br/>Facies<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Magnetic Resonance Imaging<br/>Male<br/>Phenotype<br/>Syndrome