Genome scan of Tourette syndrome in a single large pedigree shows some support for linkage to regions of chromosomes 5, 10 and 13

Psychiatric Genetics

Volumn 14, Issue 2, 2004, Pages 83-87

  Curtis, D ^a,e   Brett, P ^b   Dearlove, A M ^c   McQuillin, A ^d   Kalsi, G ^d   Robertson, M M ^d   Gurling, H M D ^d  

^a ST BARTHOLOMEW S HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c MRC UK HGMP Resource Centre   (United Kingdom)

^d ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^e ROYAL LONDON HOSPITAL   (United Kingdom)

Author keywords

Genome scan; Linkage; Tourette

Indexed keywords

ARTICLE; AUTOSOME; CHROMOSOME 10; CHROMOSOME 13; CHROMOSOME 5; CONTROLLED STUDY; GENETIC LINKAGE; GENOTYPE; GILLES DE LA TOURETTE SYNDROME; HAPLOTYPE; HUMAN; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; PEDIGREE; PRIORITY JOURNAL; SCORING SYSTEM; STATISTICAL MODEL; STATISTICAL SIGNIFICANCE; TIC;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 5; FEMALE; GENETIC MARKERS; GENOME, HUMAN; HUMANS; MALE; PEDIGREE; TOURETTE SYNDROME;

EID: 2942687716     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.ypg.0000107927.32051.f5     Document Type: Article

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