Rittinger, Olaf <br/><br/>
Clinical, cytogenetic, and molecular findings in a patient with a 46,XX,del(18)(q22)/46,XX,idic(18)(q22) karyotype.  [electronic resource] 

 -  European journal of medical genetics  Nov 2015 
 - 603-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2015.09.011  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Deletion<br/>Chromosome Duplication<br/>Chromosomes, Human, Pair 18--genetics<br/>Cleft Palate--diagnosis<br/>Craniofacial Abnormalities--diagnosis<br/>Female<br/>Heart Septal Defects, Ventricular--diagnosis<br/>Humans<br/>Infant<br/>Karyotype<br/>Mosaicism<br/>Syndrome