Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder

BMC Medical Genetics

Volumn 13, Issue , 2012, Pages

  Hooper, Sean D ^a   Johansson, Anna C V ^a   Tellgren Roth, Christian ^a   Stattin, Eva Lena ^b   Dahl, Niklas ^a   Cavelier, Lucia ^a   Feuk, Lars ^a  

^a UPPSALA UNIVERSITY   (Sweden)

^b UMEÅ UNIVERSITY   (Sweden)

Author keywords

Chromosomal translocation; Paired end sequencing; Structural variations; Tourette syndrome

Indexed keywords

ADULT; ARTICLE; AUTISM; CASE REPORT; CHIMPANZEE; CHROMOSOME 6Q; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME MAP; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; DNA DETERMINATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE REARRANGEMENT; GENETIC ASSOCIATION; GENOME; GILLES DE LA TOURETTE SYNDROME; HUMAN; MALE; OBSESSIVE COMPULSIVE DISORDER; SINGLE NUCLEOTIDE POLYMORPHISM; SPEECH DISORDER; TELOMERE;

CHROMOSOMES, HUMAN, PAIR 6; DNA COPY NUMBER VARIATIONS; ELECTRON TRANSPORT COMPLEX IV; FEMALE; GENE DELETION; GENE REARRANGEMENT; GENOME, HUMAN; HUMANS; MALE; OBSESSIVE-COMPULSIVE DISORDER; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; RECEPTORS, G-PROTEIN-COUPLED; SEQUENCE ANALYSIS, DNA; TOURETTE SYNDROME; TRANSLOCATION, GENETIC;

HOMO SAPIENS; PAN;

EID: 84871125325     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-13-123     Document Type: Article

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