메뉴 건너뛰기




Volumn 4, Issue 1, 2000, Pages 9-14

Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangements

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPING;

EID: 0034087694     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/109065700316417     Document Type: Article
Times cited : (41)

References (31)
  • 2
    • 0002425517 scopus 로고    scopus 로고
    • Subtelomeric rearrangements detected by FISH in patients with idiopathic mental retardation
    • ANDERLID, B., ANNERÉN, G., BLENNOW, E., and NORDENSKJOLD, M. (1999). Subtelomeric rearrangements detected by FISH in patients with idiopathic mental retardation. Am. J. Hum. Genet. 65 (Suppl.), A67.
    • (1999) Am. J. Hum. Genet. , vol.65 , Issue.SUPPL.
    • Anderlid, B.1    Annerén, G.2    Blennow, E.3    Nordenskjold, M.4
  • 3
    • 0011720930 scopus 로고    scopus 로고
    • Fluorescence in situ hybridization
    • S.L. Gersen and M.B. Keagle (eds.). Humana Press
    • BLANCATO, J.K. (1999). Fluorescence in situ hybridization. In The Principles of Clinical Cytogenetics. S.L. Gersen and M.B. Keagle (eds.). Humana Press, pp. 445-471.
    • (1999) The Principles of Clinical Cytogenetics , pp. 445-471
    • Blancato, J.K.1
  • 4
    • 1842415978 scopus 로고    scopus 로고
    • Previously hidden chromosome aberrations in t(12;15)-positive BALB/c plasmacytoma uncovered by multicolor spectral karyotyping
    • COLEMAN, A.E., SCHRÖCK, E., WEAVER, Z., DU MANOIR, S., YANG, F., FERGUSON-SMITH, M.A., RIED, T., and JANZ, S. (1997). Previously hidden chromosome aberrations in t(12;15)-positive BALB/c plasmacytoma uncovered by multicolor spectral karyotyping. Cancer Res. 57, 4585-4592.
    • (1997) Cancer Res. , vol.57 , pp. 4585-4592
    • Coleman, A.E.1    Schröck, E.2    Weaver, Z.3    Du Manoir, S.4    Yang, F.5    Ferguson-Smith, M.A.6    Ried, T.7    Janz, S.8
  • 5
    • 0023691590 scopus 로고    scopus 로고
    • Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes
    • CREMER, T., LICHTER, P., BORDEN, J., WARD, D.C., and MANUELIDIS, L. (1998). Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes. Hum. Genet. 80, 235-246.
    • (1998) Hum. Genet. , vol.80 , pp. 235-246
    • Cremer, T.1    Lichter, P.2    Borden, J.3    Ward, D.C.4    Manuelidis, L.5
  • 6
    • 0025120429 scopus 로고
    • Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes
    • FAN, Y.S., DAVIS, L.M., and SHOWS, T.B. (1990). Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes. Proc. Natl. Acad. Sci. USA 87, 6223-6227.
    • (1990) Proc. Natl. Acad. Sci. USA , vol.87 , pp. 6223-6227
    • Fan, Y.S.1    Davis, L.M.2    Shows, T.B.3
  • 7
    • 0033001140 scopus 로고    scopus 로고
    • Complex rearrangement of chromosome 1, 7, and 16 in chronic myelocytic leukemia
    • FAN, Y.S., RIZKALLA, K., and BARR, R.M. (1999a). Complex rearrangement of chromosome 1, 7, and 16 in chronic myelocytic leukemia. Cancer Genet. Cytogenet. 112, 190-192.
    • (1999) Cancer Genet. Cytogenet. , vol.112 , pp. 190-192
    • Fan, Y.S.1    Rizkalla, K.2    Barr, R.M.3
  • 8
    • 0032828878 scopus 로고    scopus 로고
    • A new complex variant Philadelphia chromosome, t(1;9;22)ins(17;22), characterized by fluorescence in situ hybridization in an adult ALL
    • FAN, Y.S., RIZKALLA, K., and BARR, R.M. (1999b). A new complex variant Philadelphia chromosome, t(1;9;22)ins(17;22), characterized by fluorescence in situ hybridization in an adult ALL. Leukemia Res. 23, 1001-1006.
    • (1999) Leukemia Res. , vol.23 , pp. 1001-1006
    • Fan, Y.S.1    Rizkalla, K.2    Barr, R.M.3
  • 9
    • 0033543457 scopus 로고    scopus 로고
    • Small terminal deletion of 1p and duplication of 1q: Cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years
    • FAN, Y.S., JUNG, J., and HAMILTON, B. (1999c). Small terminal deletion of 1p and duplication of 1q: cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years. Am. J. Med. Genet. 86, 118-123.
    • (1999) Am. J. Med. Genet. , vol.86 , pp. 118-123
    • Fan, Y.S.1    Jung, J.2    Hamilton, B.3
  • 12
    • 0027981573 scopus 로고
    • Rapid generation of whole chromosome painting probes (WCPs) by chromosome microdissection
    • GUAN, X.Y., MELTZER, P., and TRENT, J. (1994). Rapid generation of whole chromosome painting probes (WCPs) by chromosome microdissection. Genomics 22, 101-107.
    • (1994) Genomics , vol.22 , pp. 101-107
    • Guan, X.Y.1    Meltzer, P.2    Trent, J.3
  • 15
    • 0030960829 scopus 로고    scopus 로고
    • Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres
    • KNIGHT S.J.L., HORSLEY, S.W., REGAN, R., LANVRIE, N.M., MAHER, E.J., CARDY, D.L.N., FLINT, J., and KEARNEY, L. (1997). Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres. Eur. J. Hum. Genet. 5, 1-8.
    • (1997) Eur. J. Hum. Genet. , vol.5 , pp. 1-8
    • Knight, S.J.L.1    Horsley, S.W.2    Regan, R.3    Lanvrie, N.M.4    Maher, E.J.5    Cardy, D.L.N.6    Flint, J.7    Kearney, L.8
  • 16
    • 0001745242 scopus 로고
    • Molecular cytogenetics of continuous gene syndromes
    • C. Scriver, A. Beaudet, W. Sly, and D. Valle (eds.). McGraw Hill
    • LEDBETTER, D., and BALLABIO, A. (1995). Molecular cytogenetics of continuous gene syndromes. In The Metabolic Bases of Inherited Diseases, 7th ed. C. Scriver, A. Beaudet, W. Sly, and D. Valle (eds.). McGraw Hill, pp. 811-839.
    • (1995) The Metabolic Bases of Inherited Diseases, 7th Ed. , pp. 811-839
    • Ledbetter, D.1    Ballabio, A.2
  • 18
    • 0032195407 scopus 로고    scopus 로고
    • Clinical applications of comparative genomic hybridization
    • LEVY, B., DUNN, T.M., KAFFE, S., KARDON, N., and HIRSCHHORN, K. (1998). Clinical applications of comparative genomic hybridization. Genet. Med. 1, 4-12.
    • (1998) Genet. Med. , vol.1 , pp. 4-12
    • Levy, B.1    Dunn, T.M.2    Kaffe, S.3    Kardon, N.4    Hirschhorn, K.5
  • 23
    • 0033590672 scopus 로고    scopus 로고
    • De novo mosaic add(3) characterized to be trisomy 14q31-qter using spectral karyotyping and subtelomeric probes
    • REDDY, K.S., SULCOVA, V., YOUNG, H., BLANCATO, J.K., and HADDAD, B.R. (1999). De novo mosaic add(3) characterized to be trisomy 14q31-qter using spectral karyotyping and subtelomeric probes. Am. J. Med. Genet. 82, 318-321.
    • (1999) Am. J. Med. Genet. , vol.82 , pp. 318-321
    • Reddy, K.S.1    Sulcova, V.2    Young, H.3    Blancato, J.K.4    Haddad, B.R.5
  • 25
    • 0033559758 scopus 로고    scopus 로고
    • Spectral karyotype analysis of T-cell acute leukemia
    • ROWLEY, J.D., RESHMI, S., CARLSON, K., and ROULSTON, D. (1999). Spectral karyotype analysis of T-cell acute leukemia. Blood 93, 2038-2042.
    • (1999) Blood , vol.93 , pp. 2038-2042
    • Rowley, J.D.1    Reshmi, S.2    Carlson, K.3    Roulston, D.4
  • 29
    • 0033031587 scopus 로고    scopus 로고
    • Coexistence of several unbalanced translocations in a case of neuroblastoma: The contribution of multicolor spectral karyotyping
    • TRAKHTENBROT, L., COHEN, N., ROSNER, E., GIPSH, N., BROK-SIMONI, F., MANDEL, M., AMARIGLIO, N., and RECHAVI, G. (1999). Coexistence of several unbalanced translocations in a case of neuroblastoma: the contribution of multicolor spectral karyotyping. Cancer Genet. Cytogenet. 112, 119-123.
    • (1999) Cancer Genet. Cytogenet. , vol.112 , pp. 119-123
    • Trakhtenbrot, L.1    Cohen, N.2    Rosner, E.3    Gipsh, N.4    Brok-Simoni, F.5    Mandel, M.6    Amariglio, N.7    Rechavi, G.8
  • 30
    • 0030909689 scopus 로고    scopus 로고
    • Hidden chromosome abnormalities in haematological malignancies detected by multicolor spectral karyotyping
    • VELDMAN, T., VIGNON, C., SCHRÖCK, E., ROWLEY, J.D., and RIED, T. (1997). Hidden chromosome abnormalities in haematological malignancies detected by multicolor spectral karyotyping. Nature Genet. 15, 406-410.
    • (1997) Nature Genet. , vol.15 , pp. 406-410
    • Veldman, T.1    Vignon, C.2    Schröck, E.3    Rowley, J.D.4    Ried, T.5
  • 31
    • 0032401944 scopus 로고    scopus 로고
    • Hidden chromosome abnormalities in a primary central nervous system lymphoma detected by multicolor spectral karyotyping
    • ZATTARA-CANNONI, H., DUFOUR, H., LEPIDI, H., CHATEL, C., GRISOLI, F., and VAGNER-CAPODANO, A.M. (1998). Hidden chromosome abnormalities in a primary central nervous system lymphoma detected by multicolor spectral karyotyping. Cancer Genet. Cytogenet. 107, 98-101.
    • (1998) Cancer Genet. Cytogenet. , vol.107 , pp. 98-101
    • Zattara-Cannoni, H.1    Dufour, H.2    Lepidi, H.3    Chatel, C.4    Grisoli, F.5    Vagner-Capodano, A.M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.