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Volumn 13, Issue 6, 2001, Pages 561-565

The genetics of autism

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; CHILDHOOD DISEASE; CHROMOSOME 15Q; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 1; CHROMOSOME TRANSLOCATION 7; GENE LINKAGE DISEQUILIBRIUM; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC SCREENING; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SEX RATIO;

EID: 0035676465     PISSN: 10408703     EISSN: None     Source Type: Journal    
DOI: 10.1097/00008480-200112000-00012     Document Type: Review
Times cited : (20)

References (40)
  • 1
    • 0033837083 scopus 로고    scopus 로고
    • Practice parameter: Screening and diagnosis of autism. Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society
    • (2000) Neurology , vol.55 , pp. 468-479
    • Filipek, P.A.1    Ashwal, P.J.2    Baranek, S.3
  • 2
    • 0034609115 scopus 로고    scopus 로고
    • Autism: Progress and priorities
    • (2000) Lancet , vol.356 , pp. 490
    • Senior, K.1
  • 4
    • 0035002466 scopus 로고    scopus 로고
    • The Pediatrician's Role in the Diagnosis and Management of Autistic Spectrum Disorder in Children (RE060018)
    • (2001) Pediatrics , vol.107 , pp. 1221-1226
  • 26
    • 0034606266 scopus 로고    scopus 로고
    • Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: Identification of a BAG contig spanning the translocation breakpoint at 7q21
    • (2000) Am J Med Genet , vol.96 , pp. 749-753
    • Yan, W.1    Guan, X.Y.2    Green, E.D.3
  • 32
    • 0034606205 scopus 로고    scopus 로고
    • Analysis of 1 Mb deletion in 15q22-q23 in an autistic patient: Identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13
    • (2000) Am J Med Genet , vol.96 , pp. 765-770
    • Smith, M.1    Filipek, P.2    Wu, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.