SCOPUS 정보 검색 플랫폼

Volumn 67, Issue 2, 2000, Pages 510-514

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual

(6) Vincen, John B a Herbrick, Jo Anne a Gurling, Hugh M D b Bolton, Patrick F c Roberts, Wendy a Scherer, Stephen W a

a HOSPITAL FOR SICK CHILDREN (Canada)

b ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL (United Kingdom)

c UNIVERSITY OF CAMBRIDGE (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; AUTISM; CHROMOSOME 7Q; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; EXON; GENE MUTATION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SOCIAL INTERACTION;

DROSOPHILA MELANOGASTER; GALLUS GALLUS; SUS SCROFA;

EID: 0033859129 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/303005 Document Type: Article

Times cited : (102)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.