BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 7627929)

  • 1. Characterization by chromosome painting of balanced and unbalanced X chromosome translocations in myelodysplastic syndromes.
    Michaux L; Wlodarska I; Mecucci C; Hernandez JM; Van Orshoven A; Michaux JL; Van den Berghe H
    Cancer Genet Cytogenet; 1995 Jul; 82(1):17-22. PubMed ID: 7627929
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.
    Xu W; Li JY; Liu Q; Zhu Y; Pan JL; Qiu HR; Xue YQ
    Int J Lab Hematol; 2010 Feb; 32(1 Pt 1):e86-95. PubMed ID: 20089000
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH).
    Tosi S; Harbott J; Haas OA; Douglas A; Hughes DM; Ross FM; Biondi A; Scherer SW; Kearney L
    Leukemia; 1996 Apr; 10(4):644-9. PubMed ID: 8618441
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Is monosomy 5 an uncommon aberration? Fluorescence in situ hybridization reveals translocations and deletions in myelodysplastic syndromes or acute myelocytic leukemia.
    Bram S; Swolin B; Rödjer S; Stockelberg D; Ogärd I; Bäck H
    Cancer Genet Cytogenet; 2003 Apr; 142(2):107-14. PubMed ID: 12699885
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.
    Barbouti A; Johansson B; Höglund M; Mauritzson N; Strömbeck B; Nilsson PG; Tanke HJ; Hagemeijer A; Mitelman F; Fioretos T
    Genes Chromosomes Cancer; 2002 Oct; 35(2):127-37. PubMed ID: 12203776
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Multiplex fluorescence in situ hybridization in detecting complex chromosomal aberrations in myelodysplastic syndromes].
    Xiao B; Li JY; Pan JL; Ma L; Qiu HR; Wu YF; Xue YQ
    Zhonghua Xue Ye Xue Za Zhi; 2005 Sep; 26(9):513-6. PubMed ID: 16468325
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unbalanced translocation der(11)t(11;12)(q23;q13): a new recurrent cytogenetic aberration in myelodysplastic syndrome with a complex karyotype.
    Yamamoto K; Hato A; Minagawa K; Yakushijin K; Urahama N; Gomyo H; Sada A; Okamura A; Ito M; Matsui T
    Cancer Genet Cytogenet; 2004 Nov; 155(1):67-73. PubMed ID: 15527905
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Unbalanced 1q whole-arm translocation resulting in der(14)t(1;14)(q11-12;p11) in myelodysplastic syndrome.
    Fogu G; Campus PM; Cambosu F; Moro MA; Sanna R; Fozza C; Nieddu RM; Longinotti M; Montella A
    Cytogenet Genome Res; 2012; 136(4):256-63. PubMed ID: 22571950
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Several chromosomes involved in translocations with chromosome 5 shown with fluorescence in situ hybridization in patients with malignant myeloid disorders.
    Bram S; Rödjer S; Swolin B
    Cancer Genet Cytogenet; 2004 Nov; 155(1):74-8. PubMed ID: 15527906
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Refining the Breakpoints of Three New Translocations Identified in Myelodysplastic Syndromes.
    Costa D; Muñoz C; Carrió A; Arias A; Gómez C; Solé F; Espinet B; Azaceta G; Calasanz MJ; Nomdedeu M; Calvo X; Campo E; Nomdedeu B
    Acta Haematol; 2016; 135(2):94-100. PubMed ID: 26509426
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complex structural involvement of chromosome 7 in primary myelodysplastic syndromes determined by fluorescence in situ hybridization.
    Sessarego M; Fugazza G; Gobbi M; Bruzzone R; Bisio R; Ghio R; Patrone F
    Cancer Genet Cytogenet; 1998 Oct; 106(2):110-5. PubMed ID: 9797774
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Abnormalities of chromosome 17 in myeloid malignancies with complex chromosomal abnormalities].
    Zhu Y; Xu W; Liu Q; Pan J; Qiu H; Wang R; Qiao C; Jiang Y; Zhang S; Fan L; Zhang J; Shen Y; Xue Y; Li J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):579-82. PubMed ID: 18841577
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Correlation of cytogenetic, molecular cytogenetic, and clinical findings in 59 patients with ANLL or MDS and abnormalities of the short arm of chromosome 12.
    Streubel B; Sauerland C; Heil G; Freund M; Bartels H; Lengfelder E; Wandt H; Ludwig WD; Nowotny H; Baldus M; Grothaus-Pinke B; Büchner T; Fonatsch C
    Br J Haematol; 1998 Mar; 100(3):521-33. PubMed ID: 9504635
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Cytogenetic profile of myelodysplastic syndromes with complex karyotypes: an analysis using spectral karyotyping.
    Martínez-Ramírez A; Urioste M; Alvarez S; Vizmanos JL; Calasanz MJ; Cigudosa JC; Benítez J
    Cancer Genet Cytogenet; 2004 Aug; 153(1):39-47. PubMed ID: 15325092
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [WHO classification and cytogenetic analysis of 435 cases with myelodysplastic syndrome].
    Wang XQ;
    Zhonghua Nei Ke Za Zhi; 2008 Jun; 47(6):464-7. PubMed ID: 19040061
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A multimodal approach in the diagnosis of patients with hematopoietic disorders.
    Mark HF; Gray Y; Mark Y; Khorsand J; Sikov W
    Cancer Genet Cytogenet; 1999 Feb; 109(1):14-20. PubMed ID: 9973954
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Myelodysplastic syndrome with a t(2;11)(p21;q23-24) and translocation breakpoint close to miR-125b-1.
    Thorsen J; Aamot HV; Roberto R; Tjønnfjord GE; Micci F; Heim S
    Cancer Genet; 2012 Oct; 205(10):528-32. PubMed ID: 22944560
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A group of previously not recognized cytogenetic abnormalities in myeloid hematological malignancies.
    Chen Z; Richkind K; Roherty S; Velasco J; Lytle C; Brothman AR; Sandberg AA
    Cancer Genet Cytogenet; 1999 Sep; 113(2):162-5. PubMed ID: 10484984
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.