Taylor, L D <br/><br/>
9p monosomy in a patient with Gilles de la Tourette's syndrome.  [electronic resource] 

 -  Neurology  Sep 1991 
 - 1513-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.41.9.1513  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Chromosomes, Human, Pair 9<br/>DNA Probes<br/>Humans<br/>Interferon Type I--genetics<br/>Karyotyping<br/>Male<br/>Monosomy<br/>Polymorphism, Restriction Fragment Length<br/>Tourette Syndrome--complications