Ramelli, Gian Paolo <br/><br/>
Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study.  [electronic resource] 

 -  Developmental medicine and child neurology  Dec 2008 
 - 953-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1469-8749 
<br/><br/><label>Standard No.: </label>10.1111/j.1469-8749.2008.03048.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Autistic Disorder--diagnosis<br/>Cell Cycle Proteins--genetics<br/>Child, Preschool<br/>Chromosomes, Human, Pair 22--genetics<br/>Consanguinity<br/>Developmental Disabilities--diagnosis<br/>DiGeorge Syndrome--diagnosis<br/>Diagnosis, Differential<br/>Gene Duplication<br/>Genetic Heterogeneity<br/>Histone Chaperones<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Male<br/>Phenotype<br/>Transcription Factors--genetics