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 *

103 related articles for article (PubMed ID: 23926007)

  • 21. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies.
    Frenny VJ; Antonella Z; Luisa A; Shah AD; Sheth JJ; Rocchi M
    Indian J Cancer; 2003; 40(4):135-9. PubMed ID: 14716109
    [TBL] [Abstract][Full Text] [Related]  

  • 22. M-FISH applications in clinical genetics.
    Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
    Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Delineation of three structural Y chromosome aberrations combined molecular techniques].
    Tu XD; Zeng J; Cong XW; Yan AZ; Huang WJ; Lin YH; Zheng DZ; Zhang M; Wang ZH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):420-4. PubMed ID: 23926008
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. [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]  

  • 26. Cytogenetic features of 5q deletion and 5q- syndrome in myelodysplastic syndrome in Korea; marker chromosomes proved to be chromosome 5 with interstitial deletion by fluorescence in situ hybridization.
    Lee HR; Oh B; Hong DS; Zang DY; Yoon HJ; Kim HJ; Kim I; Ahn JS; Cheong JW; Lee KA; Cho KS; Lee MH; Bang SM; Kim TY; Yun YM; Min YH; Lee YK; Lee DS;
    Cancer Genet Cytogenet; 2010 Dec; 203(2):193-202. PubMed ID: 21156233
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Application of fluorescence in situ hybridization in prenatal diagnosis of complex chromosomal abnormalities].
    Shen YY; Li J; Kong H; Wu HN; Wu Q; Ge YS; Huang XL; Zhou YL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):529-32. PubMed ID: 19806574
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Identification of human small supernumerary marker chromosomes and discussion of its research value].
    Ou J; Wang W; Duan CY; Fu WY; Liu YL; Sun J; Zhong HL; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):91-4. PubMed ID: 23450489
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization].
    Wang H; Li H; Wang H; Wang H; Xia Y; Wen J; Long Z; Dai H; Liang D; Xia J; Wu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):538-41. PubMed ID: 18841567
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Study of two cases of prenatally detected small supernumerary marker chromosomes].
    Zeng Y; Fan J; Xu P; Zhang L; Qian F; Luo T
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug; 33(4):498-500. PubMed ID: 27455006
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
    Zunino A; Viaggi S; Ottaggio L; Fronza G; Schenone A; Roncella S; Abbondandolo A
    Haematologica; 2000 Mar; 85(3):250-5. PubMed ID: 10702812
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Sperm-fluorescence in situ hybridization analysis in patients with pericentric inversions of Y chromosome].
    Luo YQ; Qian YL; Lu HM; Xu CM; Jin F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):54-6. PubMed ID: 19199252
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical applications of primed in situ labelling (PRINS) rapid identification of a marker chromosome in a fetus.
    Velagaleti GV; Carpenter NJ; Tharapel AT
    Ann Genet; 1997; 40(3):154-7. PubMed ID: 9401104
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Application of fluorescence in situ hybridization in the diagnosis of genetic diseases].
    Zhao L; Li H; Xue YQ; Pan JL; Wu YF; Lu M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):611-4. PubMed ID: 15583994
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
    Schoch C; Haferlach T; Bursch S; Gerstner D; Schnittger S; Dugas M; Kern W; Löffler H; Hiddemann W
    Genes Chromosomes Cancer; 2002 Sep; 35(1):20-9. PubMed ID: 12203786
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Fluorescence in situ hybridization identifies complex chromosomal aberrations in multiple myeloma].
    Liu SY; Huang JW; Zhang J; Du HP; Jiang H; Li JY; Xue YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):685-8. PubMed ID: 18067084
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Incidence of numerical chromosome aberrations in meningioma tumors as revealed by fluorescence in situ hybridization using 10 chromosome-specific probes.
    Sayagués JM; Tabernero MD; Maillo A; Díaz P; Rasillo A; Bortoluci A; Gomez-Moreta J; Santos-Briz A; Morales F; Orfao A
    Cytometry; 2002 Jun; 50(3):153-9. PubMed ID: 12116338
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Molecular genetics in chronic myeloid leukemia with variant Ph translocation].
    Wu W; Li JY; Zhu Y; Qiu HR; Pan JL; Xu W; Chen LJ; Shen YF; Xue YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):470-3. PubMed ID: 17680547
    [TBL] [Abstract][Full Text] [Related]  

  • 39. FISH analysis for apparently simple terminal deletions of the X chromosome: identification of hidden structural abnormalities.
    Ogata T; Matsuo N; Fukushima Y; Saito M; Nose O; Miharu N; Uehara S; Ishizuka B
    Am J Med Genet; 2001 Dec; 104(4):307-11. PubMed ID: 11754066
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Case reports of patients with a marker chromosome].
    Kocárek E; Novotná D; Maríková T; Cernáková I; Losan F; Balícek P; Baxová A; Havlovicová M; Goetz P
    Cas Lek Cesk; 2004; 143(10):708-11; discussion 711-2. PubMed ID: 15584624
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.