Ergün, Mehmet A <br/><br/>
A case with de novo inv dup del(8p) associated with dextrocardia and corpus callosum agenesis.  [electronic resource] 

 -  Pediatrics international : official journal of the Japan Pediatric Society  Oct 2010 
 - 845-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1442-200X 
<br/><br/><label>Standard No.: </label>10.1111/j.1442-200X.2010.03181.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Agenesis of Corpus Callosum<br/>Chromosome Deletion<br/>Chromosome Inversion<br/>Chromosomes, Human, Pair 8<br/>Consanguinity<br/>Cytogenetics--methods<br/>Dextrocardia--diagnosis<br/>Female<br/>Humans<br/>Infant, Newborn<br/>Intellectual Disability--diagnosis<br/>Microarray Analysis<br/>Rare Diseases