Kamien, Benjamin <br/><br/>
Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy: additional information.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jun 2015 
 - 1424 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.36846  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Autism Spectrum Disorder--genetics<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 15<br/>Epilepsy--genetics<br/>Fathers<br/>Gene Deletion<br/>Gene Expression<br/>Humans<br/>Inheritance Patterns<br/>Male<br/>Middle Aged<br/>Sialyltransferases--deficiency