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Volumn 19, Issue 3, 2004, Pages 179-181

Duplication 15q14 → pter: A rare chromosomal abnormality underlying bipolar affective disorder

Author keywords

Bipolar psychosis; Chromosomal aberration; Chromosome 15; Familial translocation; Prader Willi syndrome

Indexed keywords

NEUROLEPTIC AGENT; RISPERIDONE; VALPROIC ACID;

EID: 2442706225     PISSN: 09249338     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.eurpsy.2004.03.001     Document Type: Article
Times cited : (8)

References (10)
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    • Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy
    • Boer H., Holland A., Whittington J., Butler J., Webb T., Clarke D. Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy. Lancet. 359:2002;135-136
    • (2002) Lancet , vol.359 , pp. 135-136
    • Boer, H.1    Holland, A.2    Whittington, J.3    Butler, J.4    Webb, T.5    Clarke, D.6
  • 3
    • 0029656217 scopus 로고    scopus 로고
    • The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q
    • Casaubon L.K., Melanson M., Lopes-Cendes I., Marineau C., Andermann E., Andermann F., et al. The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q. Am J Hum Genet. 58:1996;28-34
    • (1996) Am J Hum Genet , vol.58 , pp. 28-34
    • Casaubon, L.K.1    Melanson, M.2    Lopes-Cendes, I.3    Marineau, C.4    Andermann, E.5    Andermann, F.6
  • 5
    • 0024243972 scopus 로고
    • Duplication 8q24.2→qter and 15q14→pter resulting from a 3:1 meiotic segregation of a maternal reciprocal translocation
    • Kausch K., Haaf T., Schmid M. Duplication 8q24.2→qter and 15q14→pter resulting from a 3:1 meiotic segregation of a maternal reciprocal translocation. Am J Med Genet. 31:1988;981-985
    • (1988) Am J Med Genet , vol.31 , pp. 981-985
    • Kausch, K.1    Haaf, T.2    Schmid, M.3
  • 6
    • 0035829960 scopus 로고    scopus 로고
    • Suggestive evidence for linkage of schizophrenia to markers at chromosome 15q13-14 in Taiwanese families
    • Liu C.M., Hwu H.G., Lin M.W., Ou-Yang W.C., Lee S.F., Fann C.S., et al. Suggestive evidence for linkage of schizophrenia to markers at chromosome 15q13-14 in Taiwanese families. Am J Med Genet. 105:2001;658-661
    • (2001) Am J Med Genet , vol.105 , pp. 658-661
    • Liu, C.M.1    Hwu, H.G.2    Lin, M.W.3    Ou-Yang, W.C.4    Lee, S.F.5    Fann, C.S.6
  • 7
    • 0034640677 scopus 로고    scopus 로고
    • Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15
    • Olander E., Stamberg J., Steinberg L., Wulfsberg E.A. Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15. Am J Med Genet. 93:2000;215-218
    • (2000) Am J Med Genet , vol.93 , pp. 215-218
    • Olander, E.1    Stamberg, J.2    Steinberg, L.3    Wulfsberg, E.A.4
  • 8
    • 0033754079 scopus 로고    scopus 로고
    • Splitting schizophrenia: Periodic catatonia-susceptibility locus on chromosome 15q15
    • Stöber G., Saar K., Rüschendorf F., Meyer J., Nürnberg G., Jatzke S., et al. Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15. Am J Hum Genet. 67:2000;1201-1207
    • (2000) Am J Hum Genet , vol.67 , pp. 1201-1207
    • Stöber, G.1    Saar, K.2    Rüschendorf, F.3    Meyer, J.4    Nürnberg, G.5    Jatzke, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.