Van Esch, Hilde <br/><br/>
Developmental delay and connective tissue disorder in four patients sharing a common microdeletion at 6q13-14.  [electronic resource] 

 -  Journal of medical genetics  Oct 2010 
 - 717-20 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.2010.077586  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 6--genetics<br/>Comparative Genomic Hybridization<br/>Connective Tissue Diseases--genetics<br/>Developmental Disabilities--genetics<br/>Female<br/>Humans<br/>Infant<br/>Male<br/>Oligonucleotide Array Sequence Analysis