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Journal Abstract Search

303 related items for PubMed ID: 6607706

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. [Chromosomal changes in ovarian cancer studied by means of differential chromosome staining].
    Chudina AP, Pichugina MN.
    Vopr Onkol; 1980 Jan; 26(3):88-91. PubMed ID: 6154387
    [No Abstract] [Full Text] [Related]

  • 4. [Refractory anemias and chromosome abnormalities. A new approach of preleukemic conditions].
    Moretti G, Broustet A, Moulinier J, Veyret V, Beylot J, Paccalin J, Garcia J.
    Bord Med; 1972 Mar; 5(6):661-8. PubMed ID: 4506247
    [No Abstract] [Full Text] [Related]

  • 5. Chromosome examinations on a six-hour culture of unstimulated peripheral blood from a patient with childhood erythroleukaemia.
    Selypes A, László A, Virág I.
    Haematologia (Budap); 1989 Mar; 22(1):19-24. PubMed ID: 2707646
    [Abstract] [Full Text] [Related]

  • 6. [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 Mar; 16(2):17-21. PubMed ID: 7101445
    [Abstract] [Full Text] [Related]

  • 7. Nonrandom chromosomal changes in transitional cell carcinoma of the bladder.
    Gibas Z, Prout GR, Connolly JG, Pontes JE, Sandberg AA.
    Cancer Res; 1984 Mar; 44(3):1257-64. PubMed ID: 6692407
    [Abstract] [Full Text] [Related]

  • 8. [Congenital chromosomal anomalies in 2 children with acute lymphoblastic leukemia].
    Werner-Favre C, Cabrol C, Wyss M, Engel E.
    J Genet Hum; 1983 Mar; 31(1):49-51. PubMed ID: 6578297
    [No Abstract] [Full Text] [Related]

  • 9. Myeloid and erythroid lineage expression of haemopoietic progenitors derived from an abnormal clone in erythroleukaemia.
    Suda T, Sato Y, Furukawa Y, Suda J, Eguchi M, Saito M, Miura Y.
    Br J Haematol; 1986 Dec; 64(4):647-56. PubMed ID: 3467787
    [Abstract] [Full Text] [Related]

  • 10. [Chromosomal abnormalities of the blastic phase of chronic myeloid leukemia].
    Stoll C.
    Pathol Biol (Paris); 1982 Nov; 30(9):755-8. PubMed ID: 6760078
    [Abstract] [Full Text] [Related]

  • 11. De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19.
    Cigudosa JC, Odero MD, Calasanz MJ, Solé F, Salido M, Arranz E, Martínez-Ramirez A, Urioste M, Alvarez S, Cervera JV, MacGrogan D, Sanz MA, Nimer SD, Benitez J.
    Genes Chromosomes Cancer; 2003 Apr; 36(4):406-12. PubMed ID: 12619165
    [Abstract] [Full Text] [Related]

  • 12. Cytogenetic and immunologic abnormalities related to leukemia.
    Hirschhorn K.
    Proc Natl Cancer Conf; 1970 Apr; 6():107-12. PubMed ID: 5460544
    [No Abstract] [Full Text] [Related]

  • 13. 5q-anomaly in a patient with erythroleukemia (M6-FAB classification).
    Donti E, Mecucci C, Rosetti A, Tabilio A, Venti G.
    Haematologica; 1985 Apr; 70(5):424-7. PubMed ID: 3937779
    [No Abstract] [Full Text] [Related]

  • 14. [Chromosome anomalies in acute lymphoblastic leukemia].
    Frocrain-Herchkovitch C.
    Sem Hop; 1983 May 26; 59(21):1633-40. PubMed ID: 6310779
    [Abstract] [Full Text] [Related]

  • 15. T-cell acute lymphoblastic leukaemia with late developing Philadelphia chromosome.
    Miller BA, Reid MM, Nell M, Lipton JM, Sallan SE, Nathan DG, Tantravahi R.
    Br J Haematol; 1984 Jan 26; 56(1):139-46. PubMed ID: 6608369
    [Abstract] [Full Text] [Related]

  • 16. [Chronic lymphatic leukemia and chromosomic anomalies (author's transl)].
    Catena R, Vittuari G.
    Quad Sclavo Diagn; 1980 Dec 26; 15(4):1135-40. PubMed ID: 7454966
    [Abstract] [Full Text] [Related]

  • 17. 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 26; 38(1):73-80. PubMed ID: 6345474
    [Abstract] [Full Text] [Related]

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  • 20. [Cytogenetic studies on chronic myelocytic leukemia. Evolution of clones with additional Ph1 chromosome detected by a large number of karyotype analysis].
    Tanaka K, Kamada N, Oguma N, Takimoto Y, Kuramoto A, Ohkita T.
    Rinsho Ketsueki; 1984 Nov 26; 25(11):1778-87. PubMed ID: 6598207
    [No Abstract] [Full Text] [Related]

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