Brenk, Christian H <br/><br/>
Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.  [electronic resource] 

 -  European journal of human genetics : EJHG  Jan 2007 
 - 35-44 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.5201718  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child, Preschool<br/>Chromosome Breakage<br/>Chromosome Deletion<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 18<br/>Chromosomes, Human, Pair 20<br/>Face<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Male<br/>Phenotype<br/>Syndrome<br/>Translocation, Genetic