van Bon, B W M <br/><br/>
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.  [electronic resource] 

 -  Journal of medical genetics  Aug 2009 
 - 511-23 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.2008.063412  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosome Aberrations<br/>Chromosome Deletion<br/>Chromosome Disorders--genetics<br/>Chromosomes, Human, Pair 15--genetics<br/>Female<br/>Gene Duplication<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Intellectual Disability--genetics<br/>Male<br/>Oligonucleotide Array Sequence Analysis<br/>Pedigree<br/>Pregnancy<br/>Syndrome