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Your search keyword '"trisomy"' showing total 1,249 results

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1,249 results on '"trisomy"'

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1. A surface plasmon resonance–based technical platform for the detection of chromosome aneuploidy

2. Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders

3. Cytogenetic manifestation of chromosome 11 duplication/amplification in acute myeloid leukemia

4. Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia

5. Telomere aggregates in trisomy 21 amniocytes

6. Detection of chromosomal abnormalities associated with chronic lymphocytic leukemia: what is the best method?

7. Gain of chromosome arm 1q in patieznts in relapse and progression of multiple myeloma

8. Frequency of 5′IGH deletions in B-cell chronic lymphocytic leukemia

9. Poor outcome in a pediatric patient with acute myeloid leukemia associated with a variant t(8;21) and trisomy 6

10. Translocation (14;14)(q11;q32) with simultaneous involvement of the IGH and CEBPE genes in B-lineage acute lymphoblastic leukemia

11. Automated four-color interphase fluorescence in situ hybridization approach for the simultaneous detection of specific aneuploidies of diagnostic and prognostic significance in high hyperdiploid acute lymphoblastic leukemia

12. Blast cells with nuclear extrusions in the form of micronuclei are associated with MYC amplification in acute myeloid leukemia

13. Trisomy 8 in B-cell chronic lymphocytic leukemia

14. Loss of the extra chromosome 21 in a patient with Down syndrome and myelodysplasia

15. Distinct structural abnormalities of chromosomes 11 and 12 associated with loss of heterozygosity in X-ray-induced mouse thymic lymphomas

16. A novel t(8;18)(q13;q21) in acute monocytic leukemia evolving from constitutional trisomy 8 mosaicism

17. Trisomy 7 in postoperative spindle cell nodules

18. Characterization of trisomy 8 in pediatric undifferentiated sarcomas using advanced molecular cytogenetic techniques

19. Multipoint interphase FISH in childhood T-acute lymphoblastic leukemia detects subpopulations that carry different chromosome 3 aberrations

20. Down syndrome with low hypodiploidy in precursor B-cell acute lymphoblastic leukemia

21. Clinical, immunophenotypic, and molecular profiling of trisomy 12 in chronic lymphocytic leukemia and comparison with other karyotypic subgroups defined by cytogenetic analysis

22. Unusual type of TLS/FUS-ERG chimeric transcript in a pediatric acute myelocytic leukemia with 47,XX,+10,t(16;21)(p11;q22)

23. Constitutional partial 1q trisomy mosaicism and Wilms tumor

24. Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9)

25. High incidence and intraclonal heterogeneity of chromosome 11 aberrations in patients with newly diagnosed multiple myeloma detected by multiprobe interphase FISH

26. A der(14)t(1;14)(q12;p11) in chronic myelomonocytic leukemia

27. Hematological, immunophenotypic, and cytogenetic characteristics of acute myeloblastic leukemia with trisomy 11

28. Incidence of chromosomal anomalies detected with FISH and their clinical correlations in B-chronic lymphocytic leukemia

29. Cytogenetic aberrations in spontaneous endometrial adenocarcinomas in the BDII rat model as revealed by chromosome banding and comparative genome hybridization

30. Trisomy 8 as the sole cytogenetic abnormality in a case of extraskeletal mesenchymal chondrosarcoma

31. Chromosome 7 abnormalities in acute megakaryoblastic leukemia associated with Down syndrome

32. Specificity of interphase fluorescence in situ hybridization for detection of chromosome aberrations in tumor pathology

33. Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia

34. Multicolor fluorescence in situ hybridization analysis of a synovial sarcoma of the larynx with a t(X;18)(p11.2;q11.2) and trisomies 2 and 8

35. The role of fluorescence in situ hybridization (FISH) for monitoring hematologic malignancies with BCR/ABL or ETO/AML1 rearrangement: a comparative study with FISH and G-banding on 919 consecutive specimens of hematologic malignancies

36. Trisomy 4 as the sole cytogenetic abnormality in a patient with T-cell acute lymphoblastic leukemia

37. Trisomy 4 as the sole karyotypic abnormality in a case of acute biphenotypic leukemia with T-lineage markers in minimally differentiated acute myelocytic leukemia

38. Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia

39. Molecular cytogenetic abnormalities in patients with concurrent chronic lymphocytic leukemia and multiple myeloma shown by interphase fluorescence in situ hybridization: evidence of distinct clonal origin

40. Mosaic trisomy 2 in myelodysplastic syndromes and acute myeloblastic leukemias

41. Tetrasomy 6 and 6q14 deletion are associated with better survival in hepatocellular carcinomas

42. The effect of chlorambucil treatment on cytogenetic parameters in chronic lymphocytic leukemia patients

43. Molecular cytogenetic analysis of a pleuropulmonary blastoma

44. MLL tandem duplication in two cases of acute myelocytic leukemia with unbalanced translocations

45. Double trisomy 8 and 21 in acute myelocytic leukemias, one with rearrangement of the RUNX1 gene

46. Karyotypic evolution of four novel mouse mammary carcinoma cell lines. Identification of marker chromosomes by fluorescence in situ hybridization

47. Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies

48. Derivative (7)t(7;8)(q34;q21)

49. Trisomy 21 and other chromosomal abnormalities in acute promyelocytic leukemia

50. Cytogenetic findings and clinical course in a consecutive series of Wilms tumors

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