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326 related items for PubMed ID: 18656693
1. Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization. Xu W, Lu X, Kim Y, Luo Y, Martin M, Mulvihill JJ, Li S. Cancer Genet Cytogenet; 2008 Aug; 185(1):43-6. PubMed ID: 18656693 [Abstract] [Full Text] [Related]
2. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia. Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S. Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352 [Abstract] [Full Text] [Related]
3. Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-banding. Kuchinskaya E, Heyman M, Nordgren A, Schoumans J, Staaf J, Borg A, Söderhäll S, Grandér D, Nordenskjöld M, Blennow E. Br J Haematol; 2008 Mar; 140(5):572-7. PubMed ID: 18275435 [Abstract] [Full Text] [Related]
4. High-level amplification of the RUNX1 gene in two cases of childhood acute lymphoblastic leukemia. García-Casado Z, Cervera J, Verdeguer A, Tasso M, Valencia A, Pajuelo JC, Mena-Duran AV, Barragán E, Blanes M, Bolufer P, Sanz MA. Cancer Genet Cytogenet; 2006 Oct 15; 170(2):171-4. PubMed ID: 17011991 [Abstract] [Full Text] [Related]
5. Establishment and cytogenetic characterization of a human acute lymphoblastic leukemia cell line (ALL-VG) with ETV6/ABL1 rearrangement. Baeumler J, Szuhai K, Falkenburg JH, van Schie ML, Ottmann OG, Nijmeijer BA. Cancer Genet Cytogenet; 2008 Aug 15; 185(1):37-42. PubMed ID: 18656692 [Abstract] [Full Text] [Related]
9. Interphase FISH on TEL/AML1 positive acute lymphoblastic leukemia relapses--analysis of clinical relevance of additional TEL and AML1 copy number changes. Peter A, Heiden T, Taube T, Körner G, Seeger K. Eur J Haematol; 2009 Nov 15; 83(5):420-32. PubMed ID: 19594616 [Abstract] [Full Text] [Related]
10. Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndrome. Lo KC, Chalker J, Strehl S, Neat M, Smith O, Dastugue N, Kearney L, Izraeli S, Kempski H, Cowell JK. Br J Haematol; 2008 Sep 15; 142(6):934-45. PubMed ID: 18557744 [Abstract] [Full Text] [Related]
11. Chronic lymphocytic leukaemia Is terminal del(14)(q24) a new marker for prognostic stratification? La Starza R, Barba G, Matteucci C, Crescenzi B, Romoli S, Pierini V, Beacci D, Cantaffa R, Martelli MF, Mecucci C. Leuk Res; 2006 Dec 15; 30(12):1569-72. PubMed ID: 16650893 [Abstract] [Full Text] [Related]
12. Array comparative genomic hybridization analysis of adult acute leukemia patients. Yasar D, Karadogan I, Alanoglu G, Akkaya B, Luleci G, Salim O, Timuragaoglu A, Toruner GA, Berker-Karauzum S. Cancer Genet Cytogenet; 2010 Mar 15; 197(2):122-9. PubMed ID: 20193845 [Abstract] [Full Text] [Related]
13. The detection and significance of chromosomal abnormalities in childhood acute lymphoblastic leukaemia. Harrison CJ. Blood Rev; 2001 Mar 15; 15(1):49-59. PubMed ID: 11333138 [Abstract] [Full Text] [Related]
14. Prenatal origin of TEL-AML1-positive acute lymphoblastic leukemia in children born in California. McHale CM, Wiemels JL, Zhang L, Ma X, Buffler PA, Guo W, Loh ML, Smith MT. Genes Chromosomes Cancer; 2003 May 15; 37(1):36-43. PubMed ID: 12661004 [Abstract] [Full Text] [Related]
15. Cytogenetics of paediatric and adolescent acute lymphoblastic leukaemia. Harrison CJ. Br J Haematol; 2009 Jan 15; 144(2):147-56. PubMed ID: 19006567 [Abstract] [Full Text] [Related]
16. Efficacy of high-resolution comparative genomic hybridization (HR-CGH) in detection of chromosomal abnormalities in children with acute leukaemia. Vranova V, Mentzlova D, Oltova A, Linkova V, Zezulkova D, Filkova H, Mendelova D, Sterba J, Kuglik P. Neoplasma; 2008 Jan 15; 55(1):23-30. PubMed ID: 18190236 [Abstract] [Full Text] [Related]
17. Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region. Lilljebjörn H, Heidenblad M, Nilsson B, Lassen C, Horvat A, Heldrup J, Behrendtz M, Johansson B, Andersson A, Fioretos T. Leukemia; 2007 Oct 15; 21(10):2137-44. PubMed ID: 17690704 [Abstract] [Full Text] [Related]
18. Structural and numerical abnormalities resolved in one-step analysis: the most common chromosomal rearrangements detected by comparative genomic hybridization in childhood acute lymphoblastic leukemia. Kowalczyk JR, Babicz M, Gaworczyk A, Lejman M, Winnicka D, Styka B, Jaszczuk I. Cancer Genet Cytogenet; 2010 Jul 15; 200(2):161-6. PubMed ID: 20620600 [Abstract] [Full Text] [Related]
19. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient. Ballarati L, Recalcati MP, Bedeschi MF, Lalatta F, Valtorta C, Bellini M, Finelli P, Larizza L, Giardino D. Eur J Med Genet; 2009 Jul 15; 52(4):218-23. PubMed ID: 19236961 [Abstract] [Full Text] [Related]
20. Acute lymphoblastic leukemias with normal karyotypes are not without genomic aberrations. Usvasalo A, Räty R, Harila-Saari A, Koistinen P, Savolainen ER, Vettenranta K, Knuutila S, Elonen E, Saarinen-Pihkala UM. Cancer Genet Cytogenet; 2009 Jul 15; 192(1):10-7. PubMed ID: 19480931 [Abstract] [Full Text] [Related] Page: [Next] [New Search]