Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder

Human Genetics

Volumn 113, Issue 2, 2003, Pages 154-161

  Crawford, Fiona C ^a   Ait Ghezala, Ghania ^a   Morris, Mark ^b   Sutcliffe, Maxine J ^d   Hauser, Robert A ^c   Silver, Archie A ^a   Mullan, Michael J ^e  

^a UNIVERSITY OF SOUTH FLORIDA   (United States)

^b H LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE   (United States)

^c UNIVERSITY OF SOUTH FLORIDA   (United States)

^d UNIVERSITY OF SOUTH FLORIDA   (United States)

^e ROSKAMP INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; BEHAVIOR DISORDER; CHROMOSOME 8; CHROMOSOME BAND; CHROMOSOME BREAKAGE; CHROMOSOME ISOLATION; CHROMOSOME TRANSLOCATION 8; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DNA FLANKING REGION; FAMILY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE IDENTIFICATION; GENE MAPPING; GENETIC LINKAGE; GENETIC MARKER; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; GILLES DE LA TOURETTE SYNDROME; HUMAN; HUMAN CELL; INHERITANCE; LEARNING DISORDER; LYMPHOCYTE; MALE; MOLECULAR CLONING; MOTOR COORDINATION; MOTOR DYSFUNCTION; MUSCLE HYPOTONIA; PEDIGREE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SPEECH DISORDER; YEAST ARTIFICIAL CHROMOSOME;

EID: 0037559358     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-003-0942-4     Document Type: Article

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