Naoufal, Rania <br/><br/>
Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.  [electronic resource] 

 -  European journal of medical genetics  Sep 2016 
 - 483-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2016.07.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosome Aberrations<br/>Chromosome Deletion<br/>Chromosome Disorders--genetics<br/>Chromosomes, Human, Pair 22--genetics<br/>Comparative Genomic Hybridization--methods<br/>Developmental Disabilities--genetics<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Language Development Disorders--genetics<br/>Male<br/>Mosaicism<br/>Trisomy--genetics<br/>Uniparental Disomy--genetics