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Journal Abstract Search
418 related items for PubMed ID: 16697122
1. Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes. Paulsson K, Johansson B. Pathol Biol (Paris); 2007 Feb; 55(1):37-48. PubMed ID: 16697122 [Abstract] [Full Text] [Related]
2. Partial tandem duplication of ALL1 as a recurrent molecular defect in acute myeloid leukemia with trisomy 11. Caligiuri MA, Strout MP, Schichman SA, Mrózek K, Arthur DC, Herzig GP, Baer MR, Schiffer CA, Heinonen K, Knuutila S, Nousiainen T, Ruutu T, Block AW, Schulman P, Pedersen-Bjergaard J, Croce CM, Bloomfield CD. Cancer Res; 1996 Mar 15; 56(6):1418-25. PubMed ID: 8640834 [Abstract] [Full Text] [Related]
4. High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration. Paulsson K, Heidenblad M, Strömbeck B, Staaf J, Jönsson G, Borg A, Fioretos T, Johansson B. Leukemia; 2006 May 15; 20(5):840-6. PubMed ID: 16498392 [Abstract] [Full Text] [Related]
5. [Clinical and experimental study of 38 cases with trisomy 8]. Xu WL, Jin J, Chen ZM, Lou JY, Yu YB. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec 15; 20(6):528-31. PubMed ID: 14669224 [Abstract] [Full Text] [Related]
6. Single nucleotide polymorphism array-based karyotyping in acute myeloid leukemia or myelodysplastic syndrome with trisomy 8 as the sole chromosomal abnormality. Hahm C, Mun YC, Seong CM, Han SH, Chung WS, Huh J. Acta Haematol; 2013 Dec 15; 129(3):154-8. PubMed ID: 23208021 [Abstract] [Full Text] [Related]
7. Translocation (3;8)(q26;q24): a recurrent chromosomal abnormality in myelodysplastic syndrome and acute myeloid leukemia. Lin P, Medeiros LJ, Yin CC, Abruzzo LV. Cancer Genet Cytogenet; 2006 Apr 01; 166(1):82-5. PubMed ID: 16616115 [Abstract] [Full Text] [Related]
8. Trisomy 4 and ring chromosome in a patient with acute myelomonocytic leukemia. Vicari L, Sebastio L, Stanziola MC, Fasanaro A, Ferrara F. Haematologica; 1994 Apr 01; 79(1):83-5. PubMed ID: 15378955 [Abstract] [Full Text] [Related]
10. Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation. Park TS, Song J, Lee JH, Kim JS, Yang WI, Choi JR. Ann Clin Lab Sci; 2009 Apr 01; 39(2):176-81. PubMed ID: 19429805 [Abstract] [Full Text] [Related]
13. Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases. Beyer V, Mühlematter D, Parlier V, Cabrol C, Bougeon-Mamin S, Solenthaler M, Tobler A, Pugin P, Gregor M, Hitz F, Hess U, Chapuis B, Laurencet F, Schanz U, Schmidt PM, van Melle G, Jotterand M. Cancer Genet Cytogenet; 2005 Jul 15; 160(2):97-119. PubMed ID: 15993266 [Abstract] [Full Text] [Related]
14. Cytogenetic findings in adult greek myelodysplastic syndrome patients: predominance of single trisomy 8. Panani AD. In Vivo; 2006 Jul 15; 20(1):115-8. PubMed ID: 16433038 [Abstract] [Full Text] [Related]
16. Cytogenetic analysis of de novo acute myeloid leukemia with trilineage myelodysplasia in comparison with myelodysplastic syndrome evolving to acute myeloid leukemia. Tamura S, Takemoto Y, Hashimoto-Tamaoki T, Mimura K, Sugahara Y, Senoh J, Furuyama JI, Kakishita E. Int J Oncol; 1998 Jun 15; 12(6):1259-62. PubMed ID: 9592183 [Abstract] [Full Text] [Related]