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Volumn 6, Issue 1, 2001, Pages 87-91

Human homolog of the mouse imprinted gene Impact resides at the pericentric region of chromosome 18 within the critical region for bipolar affective disorder

Author keywords

Bipolar disorder; Genome imprinting; Physical mapping (genetics)

Indexed keywords

ANIMAL CELL; ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 18; CONTROLLED STUDY; GENE EXPRESSION; GENE MAPPING; GENETIC CODE; GENETIC LINKAGE; GENETIC SELECTION; GENETIC SUSCEPTIBILITY; GENOME; GENOME IMPRINTING; HUMAN; HUMAN CELL; MANIC DEPRESSIVE PSYCHOSIS; MOLECULAR CLONING; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

EID: 0035133610     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.mp.4000799     Document Type: Article
Times cited : (12)

References (38)
  • 13
    • 0030966234 scopus 로고    scopus 로고
    • Genetic linkage and bipolar affective disorder: Progress and pitfalls
    • (1997) Mol Psychiatry , vol.2 , pp. 200-210
    • Baron, M.1
  • 15
    • 0031472336 scopus 로고    scopus 로고
    • Disease classification and transmission effects on linkage analyses in the NIMH1 bipolar disorder pedigrees
    • (1997) Genet Epidemiol , vol.14 , pp. 587-592
    • Collins, J.S.1    Go, R.C.2
  • 25
    • 0033997450 scopus 로고    scopus 로고
    • The impact of genomic imprinting for neuro-behavioral and developmental disorders
    • (2000) J Clin Invest , vol.105 , pp. 413-418
    • Nicholls, R.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.