Faas, B H W <br/><br/>
A new case of dup(3q) syndrome due to a pure duplication of 3qter.  [electronic resource] 

 -  Clinical genetics  Oct 2002 
 - 315-20 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1034/j.1399-0004.2002.620411.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Aberrations<br/>Chromosome Disorders<br/>Chromosomes, Human, Pair 3<br/>Face--abnormalities<br/>Heart Defects, Congenital--complications<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Intellectual Disability--complications<br/>Karyotyping<br/>Male<br/>Phenotype