Koolen, David A <br/><br/>
Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation.  [electronic resource] 

 -  European journal of human genetics : EJHG  Sep 2005 
 - 1019-24 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1018-4813 
<br/><br/><label>Standard No.: </label>10.1038/sj.ejhg.5201456  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22--genetics<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Language Development Disorders--genetics<br/>Male<br/>Molecular Biology<br/>Muscle Hypotonia<br/>Nucleic Acid Hybridization