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.
42. Preleukemia. Cytogenetic clues in some confusing disorders. Nowell PC Am J Pathol; 1977 Nov; 89(2):459-76. PubMed ID: 335894 [TBL] [Abstract][Full Text] [Related]
43. Chromosomes and causation of human cancer and leukemia. XXXIV. A case of "hypereosinophilic syndrome" with unusual cytogenetic findings in a chloroma, terminating in blastic transformation and CNS leukemia. Huang CS; Gomez GA; Kohno SI; Sokal JE; Sandberg AA Cancer; 1979 Oct; 44(4):1284-9. PubMed ID: 291466 [TBL] [Abstract][Full Text] [Related]
44. Familial myeloproliferative disease. Hematological and cytogenetic studies. Slee PH; van Everdingen JJ; Geraedts JP; te Velde J; den Ottolander GJ Acta Med Scand; 1981; 210(4):321-7. PubMed ID: 7315532 [TBL] [Abstract][Full Text] [Related]
45. [Chromosome changes in leukemia]. van der Hagen CB Tidsskr Nor Laegeforen; 1974 Nov; 94(32):2208-9. PubMed ID: 4531114 [No Abstract] [Full Text] [Related]
46. A disease with immune deficiency, skin abscesses, pancytopenia, abnormal bone marrow karyotype, and increased sister chromatid exchanges: an autosomal recessive chromosome instability syndrome? Yanabe Y; Nunoi H; Tsuchiya H; Higuchi S; Akaboshi I; Kitano A; Sasaki MS; Matsuda I Jinrui Idengaku Zasshi; 1990 Sep; 35(3):263-9. PubMed ID: 2266603 [TBL] [Abstract][Full Text] [Related]
47. Translocations involving chromosomes #3 and #12: hematologic diseases associated with abnormalities of these chromosomes. Sandberg AA; Hecht BK; Ondreyco SM; Prieto F; Hecht F Cancer Genet Cytogenet; 1982 Sep; 7(1):1-17. PubMed ID: 6754070 [TBL] [Abstract][Full Text] [Related]
48. Studies on human preleukaemia. III: Chromosomal abnormalities in aregenerative anaemia with hypercellular bone marrow. Granberg-Ohman I; Hast R; Vass L Haematologica; 1980 Aug; 65(4):421-26. PubMed ID: 6774914 [No Abstract] [Full Text] [Related]
49. Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia. Li FP; Hecht F; Kaiser-McCaw B; Baranko PV; Potter NU Cancer Genet Cytogenet; 1981 Nov; 4(3):189-96. PubMed ID: 6947857 [TBL] [Abstract][Full Text] [Related]
50. Pre-leukemia in children with a missing bone marrow C chromosome and a myeloproliferative disorder. Humbert JR; Hathaway WE; Robinson A; Peakman DC; Githens JH Br J Haematol; 1971 Dec; 21(6):705-16. PubMed ID: 5132951 [No Abstract] [Full Text] [Related]
51. Eosinophilia, chloromas and a chromosome abnormality in a patient with a myeloproliferative syndrome. Ellman L; Hammond D; Atkins L Cancer; 1979 Jun; 43(6):2410-3. PubMed ID: 287548 [TBL] [Abstract][Full Text] [Related]
52. Unusual translocations t(2;6) and t(?;22) in a child with acute myelocytic leukemia. Dev VG; Carroll AJ; Crist WM; Peterson RD; Mankad VN Cancer Genet Cytogenet; 1983 Oct; 10(2):205-8. PubMed ID: 6577941 [TBL] [Abstract][Full Text] [Related]
53. Cytogenetic characteristics of therapy-related acute nonlymphocytic leukaemia, preleukaemia and acute myeloproliferative syndrome: correlation with clinical data for 61 consecutive cases. Pedersen-Bjergaard J; Philip P Br J Haematol; 1987 Jun; 66(2):199-207. PubMed ID: 3606956 [TBL] [Abstract][Full Text] [Related]
54. Chromosome instability is associated with hypodiploid clones in myelodysplastic syndromes. Knuutila S; Teerenhovi L; Borgström GH Hereditas; 1984; 101(1):19-30. PubMed ID: 6490390 [No Abstract] [Full Text] [Related]
55. Acute nonlymphocytic leukemia, preleukemia, and acute myeloproliferative syndrome secondary to treatment of other malignant diseases. Clinical and cytogenetic characteristics and results of in vitro culture of bone marrow and HLA typing. Pedersen-Bjergaard J; Philip P; Mortensen BT; Ersbøll J; Jensen G; Panduro J; Thomsen M Blood; 1981 Apr; 57(4):712-23. PubMed ID: 7470622 [No Abstract] [Full Text] [Related]
56. Marrow chromosome studies in "preleukemia". Further correlation with clinical course. Nowell PC Cancer; 1971 Aug; 28(2):513-8. PubMed ID: 5566368 [No Abstract] [Full Text] [Related]
57. The molecular biology of myeloproliferative disorders as revealed by chromosomal abnormalities. Zeleznik-Le NJ; Nucifora G; Rowley JD Semin Hematol; 1995 Jul; 32(3):201-19. PubMed ID: 7570064 [No Abstract] [Full Text] [Related]
58. A novel RUNX1 mutation in familial platelet disorder with propensity to develop myeloid malignancies. Kirito K; Sakoe K; Shinoda D; Takiyama Y; Kaushansky K; Komatsu N Haematologica; 2008 Jan; 93(1):155-6. PubMed ID: 18166807 [TBL] [Abstract][Full Text] [Related]
59. A fatal myeloproliferative syndrome in a family with thrombocytopenia and platelet dysfunction. Luddy RE; Champion LA; Schwartz AD Cancer; 1978 May; 41(5):1959-63. PubMed ID: 274171 [TBL] [Abstract][Full Text] [Related]
60. Parental origins of chromosome 7 loss in childhood monosomy 7 syndrome. Savage P; Frenck R; Paderanga D; Emperor J; Shannon KM Leukemia; 1994 Mar; 8(3):485-9. PubMed ID: 8127152 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]