Bijlsma, E K <br/><br/>
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.  [electronic resource] 

 -  European journal of medical genetics   
 - 77-87 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Multicenter Study 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2009.03.006  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple<br/>Adolescent<br/>Adult<br/>Autistic Disorder--genetics<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 16<br/>Comparative Genomic Hybridization<br/>DNA Mutational Analysis<br/>Family Health<br/>Female<br/>Genetic Testing<br/>Humans<br/>Infant<br/>Intellectual Disability--genetics<br/>Learning Disabilities<br/>Male<br/>Speech Disorders<br/>Young Adult