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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 6831045)

  • 1. Thrombocytosis and inv(3)(q21q26).
    Mecucci C; Van den Berghe H
    Blood; 1983 May; 61(5):1027. PubMed ID: 6831045
    [No Abstract]   [Full Text] [Related]  

  • 2. Rearrangement of chromosome no. 3 in a case of preleukemia with thrombocytosis.
    Norrby A; Ridell B; Swolin B; Westin J
    Cancer Genet Cytogenet; 1982 Mar; 5(3):257-63. PubMed ID: 7066881
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome.
    Jotterand Bellomo M; Parlier V; Mühlematter D; Grob JP; Beris P
    Cancer Genet Cytogenet; 1992 Apr; 59(2):138-60. PubMed ID: 1581880
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sideroblastic anemia associated with thrombocytosis and a chromosome 3 abnormality.
    Carroll AJ; Poon MC; Robinson NC; Crist WM
    Cancer Genet Cytogenet; 1986 Jun; 22(2):183-7. PubMed ID: 3458520
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Marked thrombocytosis with chromosomal abnormalities in a patient with rheumatoid arthritis.
    Satoh M; Yamagata H; Watanabe F; Matsushita Y; Nakayama S; Murakami M; Okubo K; Handa M; Ikeda Y
    Clin Rheumatol; 1993 Dec; 12(4):529-31. PubMed ID: 8124918
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ph1 -positive CML associated with megakaryocytic hyperplasia and thrombocythemia and an abnormality of chromosome no. 3.
    Carbonell F; Hoelzer D; Thiel E; Bartl R
    Cancer Genet Cytogenet; 1982 Jun; 6(2):153-61. PubMed ID: 6955003
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Refined chromosomal localization of the human thrombopoietin gene to 3q27-q28 and exclusion as the responsible gene for thrombocytosis in patients with rearrangements of 3q21 and 3q26.
    Schnittger S; de Sauvage FJ; Le Paslier D; Fonatsch C
    Leukemia; 1996 Dec; 10(12):1891-6. PubMed ID: 8946927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unusual chromosome aberration, t(13;14)(q32;q32.3), in a case of essential thrombocythemia with extreme thrombocytosis.
    Mitev L; Georgiev G; Petrov A; Manolova Y
    Cancer Genet Cytogenet; 1996 Oct; 91(1):68-70. PubMed ID: 8908170
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Translocation t(3;3)(q21;q26) and thrombocytosis.
    Gascoyne RD; Noble MC; Kalousek DK
    Cancer Genet Cytogenet; 1986 Aug; 22(4):365. PubMed ID: 3460688
    [No Abstract]   [Full Text] [Related]  

  • 10. Essential thrombocytosis with the Philadelphia chromosome (Ph').
    Nissenblatt MJ; Gartenberg G; Lee ML; Sciorra LJ; Rose DV; Rajendra BR
    Am J Med Sci; 1986 Apr; 291(4):276-9. PubMed ID: 3706392
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Macrocytic anemia, thrombocytosis, and nonlobulated megakaryocytes (5q-syndrome): report of a case.
    Arthur TZ; Krein BM
    J Am Osteopath Assoc; 1986 Jan; 86(1):23-5. PubMed ID: 3949554
    [No Abstract]   [Full Text] [Related]  

  • 12. Chromosome aberrations including der(6)t(2;6)(p15;p21.3) and der(22)t(3;22)(p21;p11) in the evolution of essential thrombocythemia to myelofibrosis with myeloid metaplasia.
    Lazarevic V; Andersson C; Wahlin A; Golovleva I
    Cancer Genet Cytogenet; 2006 Feb; 165(1):87-9. PubMed ID: 16490605
    [No Abstract]   [Full Text] [Related]  

  • 13. A chromosomal abnormality in primary thrombocythemia.
    Zaccaria A; Tura S
    N Engl J Med; 1978 Jun; 298(25):1422-3. PubMed ID: 652012
    [No Abstract]   [Full Text] [Related]  

  • 14. Translocation t(3;20) associated with thrombocythemia in Ph-positive CML.
    Turchini MF; Travade P; De Larocque A; Geneix A; Perissel B; Malet P
    Cancer Genet Cytogenet; 1986 Feb; 20(1-2):1-4. PubMed ID: 3455853
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Absence of a specific chromosomal marker in essential thrombocythemia.
    Case DC
    Cancer Genet Cytogenet; 1984 Jun; 12(2):163-5. PubMed ID: 6722757
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Probable essential thrombocythemia associated with anemia, 5q- chromosomal anomaly and nonlobulated megakaryocytes].
    Miura O; Kakita E; Kubo I; Hirose H; Inoue K; Tomiyama J; Adachi Y; Kinugasa K
    Rinsho Ketsueki; 1984 Dec; 25(12):1947-53. PubMed ID: 6533330
    [No Abstract]   [Full Text] [Related]  

  • 17. Masked inv(3)(q21q26) in a patient with minimally differentiated acute myeloid leukemia.
    Wieser R; Schreiner U; Wollenberg B; Neubauer A; Fonatsch C; Rieder H
    Haematologica; 2001 Feb; 86(2):214-5. PubMed ID: 11224497
    [No Abstract]   [Full Text] [Related]  

  • 18. Identification of a breakpoint cluster region 3' of the ribophorin I gene at 3q21 associated with the transcriptional activation of the EVI1 gene in acute myelogenous leukemias with inv(3)(q21q26).
    Suzukawa K; Parganas E; Gajjar A; Abe T; Takahashi S; Tani K; Asano S; Asou H; Kamada N; Yokota J
    Blood; 1994 Oct; 84(8):2681-8. PubMed ID: 7919381
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetic studies on primary thrombocythaemia.
    Köpf I; Swolin B; Weinfeld A
    Hereditas; 1982; 97(2):217-20. PubMed ID: 7161119
    [No Abstract]   [Full Text] [Related]  

  • 20. 3q aberration and monosomy 7 in ANLL presenting with high platelet count and diabetes insipidus.
    La Starza R; Falzetti D; Fania C; Tabilio A; Martelli MF; Mecucci C
    Haematologica; 1994; 79(4):356-9. PubMed ID: 7806090
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.