Klopocki, Eva <br/><br/>
A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH.  [electronic resource] 

 -  European journal of pediatrics  Aug 2008 
 - 903-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6199 
<br/><br/><label>Standard No.: </label>10.1007/s00431-007-0616-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Artificial, Bacterial<br/>Chromosomes, Human, Pair 15--genetics<br/>Comparative Genomic Hybridization--methods<br/>Craniofacial Abnormalities--genetics<br/>Developmental Disabilities--genetics<br/>Fingers--abnormalities<br/>Gene Dosage<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Male<br/>Penis--abnormalities