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.
2. Cytogenetic analysis in patients with myelodysplastic syndrome. Hu N; Bian M Proc Chin Acad Med Sci Peking Union Med Coll; 1990; 5(3):135-9. PubMed ID: 2098765 [TBL] [Abstract][Full Text] [Related]
3. Myelodysplastic syndrome with isochromosome 5p and trisomy 8 after treatment of a multiple myeloma. Jimenez-Sousa MA; Ferro MT; Talavera M; Villalon C; Cabello P; Laraña J; Herrera P; Garcia Sagredo JM Cancer Genet Cytogenet; 2010 Dec; 203(2):345-7. PubMed ID: 21156257 [No Abstract] [Full Text] [Related]
5. World Health Organization classification in combination with cytogenetic markers improves the prognostic stratification of patients with de novo primary myelodysplastic syndromes. Bernasconi P; Klersy C; Boni M; Cavigliano PM; Calatroni S; Giardini I; Rocca B; Zappatore R; Caresana M; Dambruoso I; Lazzarino M; Bernasconi C Br J Haematol; 2007 May; 137(3):193-205. PubMed ID: 17408458 [TBL] [Abstract][Full Text] [Related]
6. [Detection of common chromosome abnormalities in myelodysplastic syndrome with a panel fluorescence in situ hybridization]. Shen Y; Xue Y; Li J; Pan J; Wu Y; Chen S Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):160-3. PubMed ID: 12673589 [TBL] [Abstract][Full Text] [Related]
7. Trisomy 4 and ring chromosome in a patient with acute myelomonocytic leukemia. Vicari L; Sebastio L; Stanziola MC; Fasanaro A; Ferrara F Haematologica; 1994; 79(1):83-5. PubMed ID: 15378955 [TBL] [Abstract][Full Text] [Related]
9. dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes. Alfaro R; Pérez-Granero A; Durán MA; Besalduch J; Rosell J; Bernués M Leuk Res; 2008 Jan; 32(1):159-61. PubMed ID: 17509681 [TBL] [Abstract][Full Text] [Related]
11. Cytogenetic abnormalities and therapy-related myelodysplastic syndromes in rheumatic disease. McCarthy CJ; Sheldon S; Ross CW; McCune WJ Arthritis Rheum; 1998 Aug; 41(8):1493-6. PubMed ID: 9704650 [TBL] [Abstract][Full Text] [Related]
12. Sequential observation of clinical and karyotypic evolution in a patient with myelodysplastic syndrome. Xue YQ; Guo Y; Lin BJ; Zhang GR; Lu DW; Wang MH; Gu YZ; Gong JX; Wang LX Chin Med J (Engl); 1989 Sep; 102(9):689-94. PubMed ID: 2517082 [TBL] [Abstract][Full Text] [Related]
13. Clinical impact of the clone size in MDS cases with monosomy 7 or 7q deletion, trisomy 8, 20q deletion and loss of Y chromosome. Mallo M; Luño E; Sanzo C; Cervera J; Haase D; Schanz J; García-Manero G; del Cañizo C; Sanz GF; Solé F Leuk Res; 2011 Jun; 35(6):834-6. PubMed ID: 21269692 [TBL] [Abstract][Full Text] [Related]
14. Trisomy 15 as a single autosomal abnormality in a patient with unclassifiable myelodysplastic syndromes. Sashida G; Tauchi T; Kimura Y; Ohyashiki K Cancer Genet Cytogenet; 2001 May; 127(1):91-2. PubMed ID: 11414284 [No Abstract] [Full Text] [Related]
15. Consecutive chromosomal studies in patients with myelodysplastic syndrome (MDS). Czechoslovak MDS Cooperative Group. Michalova K; Musilova J; Zemanova Z Ann Genet; 1991; 34(3-4):212-8. PubMed ID: 1809229 [TBL] [Abstract][Full Text] [Related]
16. Cytogenetic abnormalities in 532 patients with myeloid leukemias and myelodyplastic syndrome. The Czechoslovak MDS Cooperative Group. Michalová K; Musilová J; Zemanová Z Czech Med; 1990; 13(4):133-44. PubMed ID: 2081440 [TBL] [Abstract][Full Text] [Related]
17. Cytogenetics of myelodysplastic syndromes. Mecucci C; La Starza R Forum (Genova); 1999; 9(1):4-13. PubMed ID: 10101207 [TBL] [Abstract][Full Text] [Related]
18. [Detection of cytogenetic abnormalities involving chromosomes 5,7 and 8 in myelodysplastic syndromes with fluorescence in situ hybridization and its clinical significance]. Cai Y; Qin YW; Wang C; Yang J; Yan SK Zhonghua Xue Ye Xue Za Zhi; 2007 Jan; 28(1):6-10. PubMed ID: 17649717 [TBL] [Abstract][Full Text] [Related]
19. Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics. Beyer V; Castagné C; Mühlematter D; Parlier V; Gmür J; Hess U; Kovacsovics T; Meyer-Monard S; Tichelli A; Tobler A; Jacky E; Schanz U; Bargetzi M; Hagemeijer A; de Witte T; van Melle G; Jotterand M Cancer Genet Cytogenet; 2004 Jul; 152(1):29-41. PubMed ID: 15193439 [TBL] [Abstract][Full Text] [Related]
20. Autosomal mendelian disorders and microcytogenetics. de Grouchy J; Turleau C Recenti Prog Med; 1990 May; 81(5):337-43. PubMed ID: 2198645 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]