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Journal Abstract Search

169 related items for PubMed ID: 11753688

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  • 4. Frequent loss of heterozygosity on the long arm of chromosome 6: identification of two distinct regions of deletion in childhood acute lymphoblastic leukemia.
    Takeuchi S, Koike M, Seriu T, Bartram CR, Schrappe M, Reiter A, Park S, Taub HE, Kubonishi I, Miyoshi I, Koeffler HP.
    Cancer Res; 1998 Jun 15; 58(12):2618-23. PubMed ID: 9635588
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  • 6. Human ependymomas reveal frequent deletions on chromosomes 6 and 9.
    Huang B, Starostik P, Schraut H, Krauss J, Sörensen N, Roggendorf W.
    Acta Neuropathol; 2003 Oct 15; 106(4):357-62. PubMed ID: 12898154
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  • 8. Genetic analysis of childhood germ cell tumors with comparative genomic hybridization.
    Schneider DT, Schuster AE, Fritsch MK, Calaminus G, Harms D, Göbel U, Perlman EJ.
    Klin Padiatr; 2001 Oct 15; 213(4):204-11. PubMed ID: 11528555
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  • 9. Identification of four distinct regions of allelic imbalances on chromosome 1 by the combined comparative genomic hybridization and microsatellite analysis on hepatocellular carcinoma.
    Leung TH, Wong N, Lai PB, Chan A, To KF, Liew CT, Lau WY, Johnson PJ.
    Mod Pathol; 2002 Nov 15; 15(11):1213-20. PubMed ID: 12429801
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  • 11. [Allelic loss of 6q16.3 microsatellite DNA in childhood acute lymphoblastic leukemia and bioinformatics analysis].
    Yang MH, Cao LZ, Yu Y, Zhang ZX, Wang Y, Kang R, Chen Y, Tan ZH, Wu XS.
    Zhonghua Xue Ye Xue Za Zhi; 2006 May 15; 27(5):289-93. PubMed ID: 16875573
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  • 12. Genomic alterations in human mesothelioma including high resolution mapping of common regions of DNA loss in chromosome arm 6q.
    Jensen RH, Tiirikainen M, You L, Ginzinger D, He B, Uematsu K, Xu Z, Treseler P, McCormick F, Jablons DM.
    Anticancer Res; 2003 May 15; 23(3B):2281-9. PubMed ID: 12894504
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  • 13. Detailed molecular analysis of 1p36 in neuroblastoma.
    White PS, Thompson PM, Seifried BA, Sulman EP, Jensen SJ, Guo C, Maris JM, Hogarty MD, Allen C, Biegel JA, Matise TC, Gregory SG, Reynolds CP, Brodeur GM.
    Med Pediatr Oncol; 2001 Jan 15; 36(1):37-41. PubMed ID: 11464901
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  • 14. Comprehensive loss of heterozygosity analysis and identification of a novel hotspot at 3p21 in salivary gland neoplasms.
    Honjo N, Gunduz M, Fukushima K, Cengiz B, Beder LB, Gunduz E, Nagatsuka H, Xiao J, Shimizu K, Nishizaki K.
    Otolaryngol Head Neck Surg; 2007 Jul 15; 137(1):119-25. PubMed ID: 17599578
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  • 15. Genetic analysis of childhood endodermal sinus tumors by comparative genomic hybridization.
    Perlman EJ, Hu J, Ho D, Cushing B, Lauer S, Castleberry RP.
    J Pediatr Hematol Oncol; 2000 Jul 15; 22(2):100-5. PubMed ID: 10779021
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  • 16. Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival.
    Ragnarsson G, Eiriksdottir G, Johannsdottir JT, Jonasson JG, Egilsson V, Ingvarsson S.
    Br J Cancer; 1999 Mar 15; 79(9-10):1468-74. PubMed ID: 10188892
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  • 17. Biological characteristics of neuroblastoma with partial deletion in the short arm of chromosome 1.
    Hiyama E, Hiyama K, Ohtsu K, Yamaoka H, Fukuba I, Matsuura Y, Yokoyama T.
    Med Pediatr Oncol; 2001 Jan 15; 36(1):67-74. PubMed ID: 11464909
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  • 18. Multiple regions of allelic loss from chromosome arm 6q in malignant mesothelioma.
    Bell DW, Jhanwar SC, Testa JR.
    Cancer Res; 1997 Sep 15; 57(18):4057-62. PubMed ID: 9307293
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  • 19. Comprehensive analysis of chromosome 1p deletions in neuroblastoma.
    Maris JM, Guo C, Blake D, White PS, Hogarty MD, Thompson PM, Rajalingam V, Gerbing R, Stram DO, Matthay KK, Seeger RC, Brodeur GM.
    Med Pediatr Oncol; 2001 Jan 15; 36(1):32-6. PubMed ID: 11464900
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  • 20. Analysis of genomic imprinting at 1p35-36 in neuroblastoma.
    Hogarty MD, Maris JM, White PS, Guo C, Brodeur GM.
    Med Pediatr Oncol; 2001 Jan 15; 36(1):52-5. PubMed ID: 11464906
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