Brief clinical report: Candidate region for Gilles de la Tourette syndrome at 7q31

American Journal of Medical Genetics

Volumn 101, Issue 3, 2001, Pages 259-261

  Kroisel, Peter M ^a   Petek, Erwin ^a   Emberger, Werner ^a   Windpassinger, Christian ^a   Wladika, Wolfgang ^b   Wagner, Klaus ^a  

^a UNIVERSITY OF GRAZ   (Austria)

^b GENERAL HOSPITAL KLAGENFURT   (Austria)

Author keywords

Chromosome 7q; Cytogenetic analysis; Duplication; Mental retardation; Tourette syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 7Q; CHROMOSOME BANDING PATTERN; CHROMOSOME BREAKAGE; CHROMOSOME DUPLICATION; FAMILY STUDY; GENE TRANSLOCATION; GILLES DE LA TOURETTE SYNDROME; HUMAN; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; PRIORITY JOURNAL; SYNDROME DELINEATION; TIC; ADOLESCENT; CHROMOSOME 7; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; GENE DUPLICATION; GENETICS; PATHOLOGY;

ADOLESCENT; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 7; CYTOGENETIC ANALYSIS; GENE DUPLICATION; HUMANS; MALE; TOURETTE SYNDROME;

EID: 0035399866     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20010701)101:3<259::aid-ajmg1374>3.0.co;2-%23     Document Type: Article

References (7)

1. The prevalence of Gilles de la Tourette syndrome in children and adolescents with autism: A large scale study
2. Tourette syndrome in a pedigree with a 7;18 translocation: Identification of a YAC spanning the translocation breakpoint at 18q22.3
3. A prevalence study of Gilles de la Tourette syndrome in North Dakota school-age children
4. A prospective longitudinal study of Gilles de la Tourette syndrome
5. Gene location in Tourette syndrome
6. Chromosome 7q: Where autism meets language disorder