Meins, M <br/><br/>
Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome.  [electronic resource] 

 -  Journal of medical genetics  May 2003 
 - e62 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Review 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.40.5.e62  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosomes, Human, Pair 22--genetics<br/>Eye Abnormalities--genetics<br/>Gene Duplication<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Phenotype<br/>Syndrome<br/>Trisomy--genetics