A candidate region for Asperger syndrome defined by two 17p breakpoints

European Journal of Human Genetics

Volumn 11, Issue 2, 2003, Pages 189-195

  Tentler, Dmitry ^a   Johannesson, Tonnie ^b   Johansson, Maria ^b,c   Råstam, Maria ^b,c   Gillberg, Christopher ^b,c   Orsmark, Christina ^a   Carlsson, Birgit ^a   Wahlström, Jan ^b   Dahl, Niklas ^a  

^a UPPSALA UNIVERSITY   (Sweden)

^b UNIVERSITY OF GOTHENBURG   (Sweden)

^c ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

Asperger syndrome; Autism; Balanced translocation; Candidate region

Indexed keywords

RNA;

ADULT; ARTICLE; ASPERGER SYNDROME; AUTISM; CASE REPORT; CHROMOSOME 17P; CHROMOSOME TRANSLOCATION 13; CHROMOSOME TRANSLOCATION 17; CHROMOSOME TRANSLOCATION 19; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENE FUNCTION; GENE SEQUENCE; GENE STRUCTURE; GENETIC ANALYSIS; HUMAN; KARYOTYPE; LYMPHOBLASTOID CELL LINE; MALE; METAPHASE CHROMOSOME; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; SOCIAL BEHAVIOR; SOCIAL DISABILITY; SOCIAL INTERACTION;

ADOLESCENT; ADULT; ASPERGER SYNDROME; BLOTTING, NORTHERN; CHILD; CHROMOSOMES, HUMAN, PAIR 17; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; PHYSICAL CHROMOSOME MAPPING; TRANSLOCATION, GENETIC;

EID: 0037301216     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200939     Document Type: Article

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