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 *

369 related articles for article (PubMed ID: 6930118)

  • 1. A case of acute myeloblastic leukemia with chromosomes showing 46, XY = 11/46, XY, 21q- = 39.
    Tadano J; Niwa M; Nagumo F; Watanabe K; Arimori S
    Tokai J Exp Clin Med; 1980 Jan; 5(1):45-50. PubMed ID: 6930118
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemia.
    Werner-Favre C; Cabrol C; Beris P; Engel E
    Ann Genet; 1983; 26(4):240-2. PubMed ID: 6607706
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Acute myelomonocytic leukemia (M4) with eosinophilia: problems concerning chromosome 16 abnormality.
    Harth H; Pees H; Zankl H
    Cancer Genet Cytogenet; 1986 Oct; 23(2):127-33. PubMed ID: 3463402
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Y chromosome duplication in chronic myeloid leukemia.
    Stoll C; Oberling F
    Nouv Rev Fr Hematol (1978); 1982; 24(1):9-12. PubMed ID: 6951142
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Translocation (8q-; 21q+) with loss of chromosome Y in acute myeloblastic leukemia in children].
    Verellen-Dumoulin C; Vachaudez C; Libouton JM; Cornu G; Rodhain J; de Meyer R
    J Genet Hum; 1983 Mar; 31(1):57. PubMed ID: 6578299
    [No Abstract]   [Full Text] [Related]  

  • 6. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
    Schoch C; Haferlach T; Bursch S; Gerstner D; Schnittger S; Dugas M; Kern W; Löffler H; Hiddemann W
    Genes Chromosomes Cancer; 2002 Sep; 35(1):20-9. PubMed ID: 12203786
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Phenotypic disorders in balanced reciprocal translocation: karyotype 46,XY,rcp(13; 21)(q22; q22)].
    Badalian LO; Malygina NA; Gozman TV; Petrukhin AS; Mutovin GR
    Tsitol Genet; 1982; 16(2):17-21. PubMed ID: 7101445
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical implications of cytogenetic abnormalities in acute nonlymphocytic leukemia.
    Trujillo JM; Cork A
    Am J Pediatr Hematol Oncol; 1981; 3(4):425-31. PubMed ID: 7036783
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosomal aberrations in bone marrow mesenchymal stroma cells from patients with myelodysplastic syndrome and acute myeloblastic leukemia.
    Blau O; Hofmann WK; Baldus CD; Thiel G; Serbent V; Schümann E; Thiel E; Blau IW
    Exp Hematol; 2007 Feb; 35(2):221-9. PubMed ID: 17258071
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gain of an isochromosome 5p: a rare recurrent abnormality in acute myeloid leukemia.
    Panani AD
    In Vivo; 2006; 20(3):359-60. PubMed ID: 16724670
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytogenetic characterization of putative human myeloblastic leukemia cell lines (ML-1, -2, and -3): origin of the cells.
    Ohyashiki K; Ohyashiki JH; Sandberg AA
    Cancer Res; 1986 Jul; 46(7):3642-7. PubMed ID: 3458526
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial monosomy for a 21 chromosome. Report of a new case of r(21) and review of the literature.
    Ferrante E; Vignetti P; Antonelli M; Bruni L; Bertasi S; Chessa L
    Helv Paediatr Acta; 1983 Mar; 38(1):73-80. PubMed ID: 6345474
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Acute myeloblastic leukemia with involvement of the basophilic cell line and anomalies of the short arm of chromosome 12 (12p)].
    Daniel MT; Bernheim A; Flandrin G; Berger R
    C R Acad Sci III; 1985; 301(6):299-301. PubMed ID: 3928106
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Case of acute myeloblastic leukemia with Philadelphia chromosome].
    Sasaki T; Koyama R; Nishiie K; Yamamoto A; Gocho Y
    Saishin Igaku; 1970 Jan; 25(1):187-92. PubMed ID: 5271127
    [No Abstract]   [Full Text] [Related]  

  • 15. Acute lymphoblastic leukemia at relapse in a child with acute myeloblastic leukemia.
    Bernstein ML; Esseltine DW; Emond J; Vekemans M
    Am J Pediatr Hematol Oncol; 1986; 8(2):153-7. PubMed ID: 3461717
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Cytogenetic analysis and phenotype location analysis on the karyotype of a ring chromosome 21 syndrome].
    Zhu XY; Zhao R; Ye ZC; Peng YG; Tan YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):682-3. PubMed ID: 16331572
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Myeloblastic leukaemia with the Philadelphia chromosome and with osteosclerosis. Report in a child (author's transl)].
    Svarch E; Cristo E; Méndez D
    Sangre (Barc); 1978; 23(6):882-6. PubMed ID: 283556
    [No Abstract]   [Full Text] [Related]  

  • 18. Association of specific chromosome abnormalities with type of acute leukemia and with patient age.
    Rowley JD
    Cancer Res; 1981 Sep; 41(9 Pt 1):3407-10. PubMed ID: 6942914
    [TBL] [Abstract][Full Text] [Related]  

  • 19. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
    Rivera H; Rivas F; Plascencia L; Cantú JM
    Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Peculiar chromosomal pattern in a case of acute myeloblastic leukaemia in a patient with XY/XO mosaic].
    Cardini G; Clemente R; Bersi M
    Arch Sci Med (Torino); 1968 Sep; 125(9):433-8. PubMed ID: 17340799
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.