Vincent, John B <br/><br/>
Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q.  [electronic resource] 

 -  American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics  Sep 2009 
 - 817-26 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-485X 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.b.30903  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Autistic Disorder--genetics<br/>Base Sequence<br/>Chromosome Breakage<br/>Chromosomes, Human, Pair 18--genetics<br/>Chromosomes, Human, Pair 5--genetics<br/>DNA Mutational Analysis<br/>Desmocollins--genetics<br/>Humans<br/>Intracellular Signaling Peptides and Proteins<br/>Male<br/>Molecular Sequence Data<br/>Multigene Family<br/>Polymorphism, Single Nucleotide<br/>Proteins--genetics<br/>Receptors, Adrenergic, beta-2--genetics<br/>Receptors, Serotonin--genetics<br/>Translocation, Genetic