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 *

93 related articles for article (PubMed ID: 468256)

  • 21. Refractory anemia with ring sideroblasts associated with marked thrombocytosis harboring cytogenetic abnormality dup(2)(p15p22) treated with decitabine.
    Kim J; Kim YR; Lee KA
    Leuk Lymphoma; 2012 Nov; 53(11):2287-9. PubMed ID: 22468921
    [No Abstract]   [Full Text] [Related]  

  • 22. 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]  

  • 23. Further evidence for a non-random chromosomal abnormality in acute promyelocytic leukemia.
    Rowley JD; Golomb HM; Vardiman J; Fukuhara S; Dougherty C; Potter D
    Int J Cancer; 1977 Dec; 20(6):869-72. PubMed ID: 271143
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A case of 21q--syndrome with normal SOD-1 activity.
    Yamamoto Y; Ogasawara N; Gotoh A; Komiya H; Nakai H; Kuroki Y
    Hum Genet; 1979 May; 48(3):321-7. PubMed ID: 468232
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Masked Philadelphia chromosome due to the translocation (1q-;22q +) and small chromosome 19 in a case of acute leukemia.
    Suciu S; Marinca E; Gădăleanu V
    Neoplasma; 1984; 31(5):573-9. PubMed ID: 6594592
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Myelodysplastic syndrome with thrombocytosis in a patient with Klinefelter's syndrome.
    Yamauchi K
    Acta Haematol; 1993; 89(1):43-5. PubMed ID: 8480486
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
    Pai GS; Thomas GH; Leonard CO; Ward JC; Valle DL; Pyeritz RE
    Johns Hopkins Med J; 1979 Oct; 145(4):162-9. PubMed ID: 491337
    [No Abstract]   [Full Text] [Related]  

  • 28. 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]  

  • 29. Chromosomes and causation of human cancer and leukemia. XXVI. Binding studies in acute lymphoblastic leukemia (ALL).
    Oshimura M; Freeman AI; Sandberg AA
    Cancer; 1977 Sep; 40(3):1161-72. PubMed ID: 268996
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [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]  

  • 31. Acute myeloid leukemia associated with t(1;3)(p36;q21) and extreme thrombocytosis: a clinical study with literature review.
    Lim G; Kim MJ; Oh SH; Cho SY; Lee HJ; Suh JT; Lee J; Lee WI; Cho KS; Park TS
    Cancer Genet Cytogenet; 2010 Dec; 203(2):187-92. PubMed ID: 21156232
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Marked thrombocytosis following relapse of acute myeloblastic leukemia associated with development of translocation (2;14) (p13;q32).
    Tasaka T; Nagai M; Matsuhashi Y; Uehara E; Kakazu N; Abe T; Tamura T
    Leuk Lymphoma; 2002 Oct; 43(10):2063-5. PubMed ID: 12481911
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Partial trisomy and monosomy 21 in an infant with an unusual de novo 21/21 translocation.
    Cantu JM; Hernandez A; Plascencia L; Vaca G; Moller M; Rivera H
    Ann Genet; 1980; 23(3):183-6. PubMed ID: 6448566
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. [Abnormality of chromosome number 1 in 3 cases of acute transformation of chronic myeloid leukemia].
    Smadja N; Krulik M; Génot JY; Audebert AA; Debray J
    Nouv Rev Fr Hematol (1978); 1984; 26(5):303-8. PubMed ID: 6594670
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement.
    Tharapel AT; Redheendran R; Mankinen CB; Kukolich MK
    J Med Genet; 1984 Oct; 21(5):391-5. PubMed ID: 6239037
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Falsely high erythrocyte and leucocyte counts related to extreme thrombocytosis in a patient with a 5 q-syndrome.
    Ciaudo M; Bernadou A; Samama M; Lecompte T
    Clin Lab Haematol; 1994 Mar; 16(1):91-3. PubMed ID: 8039355
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.