These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

239 related articles for article (PubMed ID: 17072374)

  • 1. Assessment of molecular cytogenetic methods for the detection of chromosomal abnormalities.
    Une T; Yokoyama Y; Ninomiya S; Shinozuka M; Maruyama H; Morishima T
    Acta Med Okayama; 2006 Oct; 60(5):279-87. PubMed ID: 17072374
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of marker or complex chromosomal rearrangements present in pre- and post-natal karyotypes utilizing a combination of G-banding, spectral karyotyping and fluorescence in situ hybridization.
    Heng HH; Ye CJ; Yang F; Ebrahim S; Liu G; Bremer SW; Thomas CM; Ye J; Chen TJ; Tuck-Muller C; Yu JW; Krawetz SA; Johnson A
    Clin Genet; 2003 May; 63(5):358-67. PubMed ID: 12752567
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Spectral karyotyping of seven prenatally detected marker chromosomes and complex chromosome aberrations].
    Song HL; Chen BJ; Fang Q; Xie YJ; Lin SB; Wu JZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):393-7. PubMed ID: 22875493
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping.
    Veldman T; Vignon C; Schröck E; Rowley JD; Ried T
    Nat Genet; 1997 Apr; 15(4):406-10. PubMed ID: 9090389
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of recurrent chromosomal breakpoints in multiple myeloma with complex karyotypes by combined G-banding, spectral karyotyping, and fluorescence in situ hybridization analyses.
    Sáez B; Martín-Subero JI; Largo C; Martín MC; Odero MD; Prosper F; Siebert R; Calasanz MJ; Cigudosa JC
    Cancer Genet Cytogenet; 2006 Sep; 169(2):143-9. PubMed ID: 16938572
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multicolor banding technique, spectral color banding (SCAN): new development and applications.
    Kakazu N; Abe T
    Cytogenet Genome Res; 2006; 114(3-4):250-6. PubMed ID: 16954662
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spectral karyotyping study of chromosome abnormalities in human leukemia.
    Zhao L; Hayes K; Khan Z; Glassman A
    Cancer Genet Cytogenet; 2001 Jun; 127(2):143-7. PubMed ID: 11425454
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosomal rearrangements detected by FISH and G-banding.
    Hou JW; Wang TR
    J Formos Med Assoc; 1996 Sep; 95(9):686-91. PubMed ID: 8918057
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome.
    Kakazu N; Taniwaki M; Horiike S; Nishida K; Tatekawa T; Nagai M; Takahashi T; Akaogi T; Inazawa J; Ohki M; Abe T
    Genes Chromosomes Cancer; 1999 Dec; 26(4):336-45. PubMed ID: 10534769
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey.
    Karaman B; Aytan M; Yilmaz K; Toksoy G; Onal EP; Ghanbari A; Engur A; Kayserili H; Yuksel-Apak M; Basaran S
    Eur J Med Genet; 2006; 49(3):207-14. PubMed ID: 16762822
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytogenetic characterization of the TM4 mouse Sertoli cell line. I. Conventional banding techniques, FISH and SKY.
    Guttenbach M; Steinlein C; Engel W; Schmid M
    Cytogenet Cell Genet; 2001; 94(1-2):71-8. PubMed ID: 11701958
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
    Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of complex chromosomal abnormalities in B-cell lymphoma by a combined spectral karyotyping (SKY) analysis and fluorescence in situ hybridization (FISH) using a 14q telomere probe.
    Kakazu N; Kito K; Hitomi T; Oita J; Nishida K; Masuda K; Miki T; Abe T
    Am J Hematol; 2000 Dec; 65(4):291-7. PubMed ID: 11074557
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY).
    Cohen N; Betts DR; Trakhtenbrot L; Niggli FK; Amariglio N; Brok-Simoni F; Rechavi G; Meitar D
    Genes Chromosomes Cancer; 2001 Jul; 31(3):201-8. PubMed ID: 11391790
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2.
    Hilgenfeld E; Padilla-Nash H; McNeil N; Knutsen T; Montagna C; Tchinda J; Horst J; Ludwig WD; Serve H; Büchner T; Berdel WE; Schröck E; Ried T
    Br J Haematol; 2001 May; 113(2):305-17. PubMed ID: 11380393
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
    Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multicolour spectral karyotyping for complex chromosomal rearrangements in repeated abortion or congenital anomalies.
    Tanemura M; Suzumori K; Nishikawa N; Ishihara Y
    Prenat Diagn; 2001 Dec; 21(13):1123-8. PubMed ID: 11787036
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New chromosomal breakpoints in non-Hodgkin's lymphomas revealed by spectral karyotyping and G-banding.
    Nordgren A; Sørensen AG; Tinggaard-Pedersen N; Blennow E; Larsson C; Lagercrantz S
    Int J Mol Med; 2000 May; 5(5):485-92. PubMed ID: 10762651
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Combined use of molecular cytogenetic techniques to detect a small chromosomal translocation].
    Xie YJ; Chen BJ; Wu JZ; Chen Z; Lin SB; Fang Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Oct; 28(5):568-71. PubMed ID: 21983737
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of chromosomal aberrations in diffuse large B-cell lymphoma (DLBL) by G-banding and spectral karyotyping (SKY).
    Adam P; Steinlein C; Schmid M; Haralambieva E; Stocklein H; Leich E; Rosenwald A; Muller-Hermelink HK; Ott G
    Cytogenet Genome Res; 2006; 114(3-4):274-8. PubMed ID: 16954666
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.