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Volumn 128 A, Issue 2, 2004, Pages 199-203

De novo complex chromosomal rearrangements (CCR) involving chromosome 1, 5, and 6 resulting in microdeletion for 6q14 in a female carrier with psychotic disorder

Author keywords

Complex chromosomal rearrangement; High resolution CGH; Microdeletion 6q14; Obesity; Psychotic disorder

Indexed keywords

DNA; NEUROTRANSMITTER; SEROTONIN;

EID: 4344715840     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30064     Document Type: Article
Times cited : (16)

References (23)
  • 2
    • 0042121277 scopus 로고    scopus 로고
    • A systematic review of association studies investigating genes coding for serotonin receptors and the serotonin transporter: II. Suicidal behavior
    • Anguelova M, Benkelfat C, Turecki G. 2003. A systematic review of association studies investigating genes coding for serotonin receptors and the serotonin transporter: II. Suicidal behavior. Mol Psychiatry 8(7):646-653.
    • (2003) Mol Psychiatry , vol.8 , Issue.7 , pp. 646-653
    • Anguelova, M.1    Benkelfat, C.2    Turecki, G.3
  • 3
    • 0031864888 scopus 로고    scopus 로고
    • De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: Report and review
    • Batanian JR, Eswara MS. 1998. De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: Report and review. Am J Med Genet 78(1):44-51.
    • (1998) Am J Med Genet , vol.78 , Issue.1 , pp. 44-51
    • Batanian, J.R.1    Eswara, M.S.2
  • 4
    • 0028043602 scopus 로고
    • Molecular analysis of a complex chromosomal rearrangement and a review of familial cases
    • Batista DA, Pai GS, Stetten G. 1994. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases. Am J Med Genet 53:255-263.
    • (1994) Am J Med Genet , vol.53 , pp. 255-263
    • Batista, D.A.1    Pai, G.S.2    Stetten, G.3
  • 5
    • 0018121252 scopus 로고
    • A complex translocation involving chromosomes 3,11, and 14 with an interstitial deletion del(14)(q13q22) in a child with congenital glaucoma and cleft lip and palate
    • Buchanan PD, Rao KW, Doerr CL, Aylsworth AS. 1978. A complex translocation involving chromosomes 3,11, and 14 with an interstitial deletion del(14)(q13q22) in a child with congenital glaucoma and cleft lip and palate. Birth Defects Orig Artic Ser 14:317-322.
    • (1978) Birth Defects Orig Artic Ser , vol.14 , pp. 317-322
    • Buchanan, P.D.1    Rao, K.W.2    Doerr, C.L.3    Aylsworth, A.S.4
  • 7
    • 0019522520 scopus 로고
    • High resolution R- and G-banding on the same preparation
    • Dutrillaux B, Vigas-Pequignot E. 1981. High resolution R- and G-banding on the same preparation. Hum Genet 57:93-95.
    • (1981) Hum Genet , vol.57 , pp. 93-95
    • Dutrillaux, B.1    Vigas-Pequignot, E.2
  • 8
    • 0036373344 scopus 로고    scopus 로고
    • A genomewide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26, and 16p13.3
    • Ewald H, Flint T, Kruse TA, Mors O. 2002. A genomewide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26, and 16p13.3. Mol Psychiatry 7(7):734-744.
    • (2002) Mol Psychiatry , vol.7 , Issue.7 , pp. 734-744
    • Ewald, H.1    Flint, T.2    Kruse, T.A.3    Mors, O.4
  • 9
    • 0022545607 scopus 로고
    • Balanced double complex translocations [46,XX,t(1p;6p;7p;3q;11p) (11q22p;21q)]
    • Fukushima Y, Kuroki Y, Ito T. 1986. Balanced double complex translocations [46,XX,t(1p;6p;7p;3q;11p)(11q22p;21q)]. Am J Med Genet 25:313-317.
    • (1986) Am J Med Genet , vol.25 , pp. 313-317
    • Fukushima, Y.1    Kuroki, Y.2    Ito, T.3
  • 10
    • 0034016043 scopus 로고    scopus 로고
    • Profound obesity associated with a balanced translocation that disrupts the SIM1 gene
    • Holder JL Jr, Butte NF, Zinn AR. 2000. Profound obesity associated with a balanced translocation that disrupts the SIM1 gene. Hum Mol Genet 9(1):101-108.
    • (2000) Hum Mol Genet , vol.9 , Issue.1 , pp. 101-108
    • Holder Jr., J.L.1    Butte, N.F.2    Zinn, A.R.3
  • 12
  • 15
    • 0028128949 scopus 로고
    • Assignment of the gene encoding the 5-HT1E serotonin receptor (S31) (locus HTR1E) to human chromosome 6q14-q15
    • Levy FO, Holtgreve-Grez H, Tasken K, Solberg R, Ried T, Gudermann T. 1994. Assignment of the gene encoding the 5-HT1E serotonin receptor (S31) (locus HTR1E) to human chromosome 6q14-q15. Genomics 22(3): 637-640.
    • (1994) Genomics , vol.22 , Issue.3 , pp. 637-640
    • Levy, F.O.1    Holtgreve-Grez, H.2    Tasken, K.3    Solberg, R.4    Ried, T.5    Gudermann, T.6
  • 17
    • 0019460218 scopus 로고
    • Resolution of break-points in a complex rearrangement by use of multiple staining techniques: Confirmation of suspected 12p12.3 intra-band deletion by dosage effects of LDHB
    • Magenis E, Brown MG, Chamberlain J, Donlon T, Hepburn D, Lamvik E, Lovrien E, Yoshitomi M. 1981. Resolution of break-points in a complex rearrangement by use of multiple staining techniques: Confirmation of suspected 12p12.3 intra-band deletion by dosage effects of LDHB. Am J Med Genet 9:95-103.
    • (1981) Am J Med Genet , vol.9 , pp. 95-103
    • Magenis, E.1    Brown, M.G.2    Chamberlain, J.3    Donlon, T.4    Hepburn, D.5    Lamvik, E.6    Lovrien, E.7    Yoshitomi, M.8
  • 19
    • 0034487876 scopus 로고    scopus 로고
    • A distinctive phenotype associated with an interstitial deletion 6q14 contained within a de novo pericentric inversion 6(p11.2q15)
    • Passarge E. 2000. A distinctive phenotype associated with an interstitial deletion 6q14 contained within a de novo pericentric inversion 6(p11.2q15). Cytogenet Cell Genet 91(1-4):192-198.
    • (2000) Cytogenet Cell Genet , vol.91 , Issue.1-4 , pp. 192-198
    • Passarge, E.1
  • 20
    • 0036850219 scopus 로고    scopus 로고
    • DNA variation and psychopharmacology of the human serotonin receptor 1B (HTR1B) gene
    • Sanders AR, Duan J, Gejman PV. 2002. DNA variation and psychopharmacology of the human serotonin receptor 1B (HTR1B) gene. Pharmacogenomics 3(6):745-762.
    • (2002) Pharmacogenomics , vol.3 , Issue.6 , pp. 745-762
    • Sanders, A.R.1    Duan, J.2    Gejman, P.V.3
  • 21
    • 0022005478 scopus 로고
    • A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome
    • Schwartz S, Biesel JH, Panny SR, Cohen MM. 1985. A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome. Clin Genet 27:175-182.
    • (1985) Clin Genet , vol.27 , pp. 175-182
    • Schwartz, S.1    Biesel, J.H.2    Panny, S.R.3    Cohen, M.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.