Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.

Paschou, P; Feng, Y; Pakstis, A J; Speed, W C; DeMille, M M; Kidd, J R; Jaghori, B; Kurlan, R; Pauls, D L; Sandor, P; Barr, C L; Kidd, K K

Paschou, P; Feng, Y; Pakstis, A J; Speed, W C; DeMille, M M; Kidd, J R; Jaghori, B; Kurlan, R; Pauls, D L; Sandor, P; Barr, C L; Kidd, K K.

Affiliation

Paschou P; Department of Genetics, Yale University School of Medicine, New Haven, CT 06520-8005, USA. peristera.paschou@yale.edu

Am J Hum Genet ; 75(4): 545-60, 2004 Oct.

Article in En | MEDLINE | ID: mdl-15303240

Subject(s)

Chromosomes, Human, Pair 17/genetics; Genetic Linkage; Genetic Predisposition to Disease; Tourette Syndrome/genetics; C-Reactive Protein/genetics; Chromosome Mapping; Gene Frequency; Genotype; Haplotypes/genetics; Humans; Linkage Disequilibrium/genetics; Lod Score; Microsatellite Repeats/genetics; Microtubule-Associated Proteins/genetics; Nerve Tissue Proteins/genetics; Pedigree; Polymorphism, Single Nucleotide/genetics; White People/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 17 / Tourette Syndrome / Genetic Predisposition to Disease / Genetic Linkage Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Am J Hum Genet Year: 2004 Document type: Article

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