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Journal Abstract Search

530 related items for PubMed ID: 3707294

  • 41. Chromosomal deletion and retinoblastoma.
    Knudson AG, Meadows AT, Nichols WW, Hill R.
    N Engl J Med; 1976 Nov 11; 295(20):1120-3. PubMed ID: 980006
    [No Abstract] [Full Text] [Related]

  • 42. [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]

  • 43. Temporal changes in chromosome abnormality rate in human spontaneous abortions: evidence for an association between sex-chromosome monosomy and trisomy 16.
    Hassold T, MacLean C.
    Cytogenet Cell Genet; 1984 May 26; 38(3):200-5. PubMed ID: 6541559
    [Abstract] [Full Text] [Related]

  • 44. Chromosomal reorganization for the expression of recessive mutation of retinoblastoma susceptibility gene in the development of osteosarcoma.
    Toguchida J, Ishizaki K, Sasaki MS, Ikenaga M, Sugimoto M, Kotoura Y, Yamamuro T.
    Cancer Res; 1988 Jul 15; 48(14):3939-43. PubMed ID: 2898286
    [Abstract] [Full Text] [Related]

  • 45. [Studies on deletions on chromosome 13 and their transmission in patients with retinoblastoma].
    Gao Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1991 Jun 15; 13(3):157-60. PubMed ID: 1831719
    [Abstract] [Full Text] [Related]

  • 46. Costenbader Memorial Lecture: Genesis and genetics of retinoblastoma.
    François J.
    Adv Ophthalmol; 1979 Jun 15; 39():181-209. PubMed ID: 394592
    [Abstract] [Full Text] [Related]

  • 47. Possible inactivation of part of chromosome 13 due to 13qXp translocation associated with retinoblastoma.
    Ejima Y, Sasaki MS, Kaneko A, Tanooka H, Hara Y, Hida T, Kinoshita Y.
    Clin Genet; 1982 Jun 15; 21(6):357-61. PubMed ID: 7127878
    [Abstract] [Full Text] [Related]

  • 48. Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: verification by standard staining techniques, new densitometric methods, and somatic cell hybridization.
    Squire J, Phillips RA, Boyce S, Godbout R, Rogers B, Gallie BL.
    Hum Genet; 1984 Jun 15; 66(1):46-53. PubMed ID: 6583158
    [Abstract] [Full Text] [Related]

  • 49. 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 15; 35(1):20-9. PubMed ID: 12203786
    [Abstract] [Full Text] [Related]

  • 50. Chromosome evolution and high-resolution analysis of leucocytes, bone marrow, and tumor cells of retinoblastoma patients.
    Lemieux N, Richer CL.
    Am J Med Genet; 1990 Aug 15; 36(4):456-62. PubMed ID: 2389803
    [Abstract] [Full Text] [Related]

  • 51. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M, Mutoh K, Okuno T, Mikawa H, Edagawa J, Abe T.
    Ann Genet; 1983 Aug 15; 26(2):116-9. PubMed ID: 6604486
    [Abstract] [Full Text] [Related]

  • 52. Molecular detection of constitutional deletions in patients with retinoblastoma.
    Blanquet V, Créau-Goldberg N, de Grouchy J, Turleau C.
    Am J Med Genet; 1991 Jun 01; 39(3):355-61. PubMed ID: 1867290
    [Abstract] [Full Text] [Related]

  • 53. [Retinoblastoma and interstitial deletion of 13q (author's transl)].
    De Grouchy J, Turleau C, Cabanis MO, Richardet JM.
    Arch Fr Pediatr; 1980 Oct 01; 37(8):531-5. PubMed ID: 7447607
    [Abstract] [Full Text] [Related]

  • 54. Structural genes of coagulation factors VII and X located on 13q34.
    Gilgenkrantz S, Briquel ME, André E, Alexandre P, Jalbert P, Le Marec B, Pouzol P, Pommereuil M.
    Ann Genet; 1986 Oct 01; 29(1):32-5. PubMed ID: 3487272
    [Abstract] [Full Text] [Related]

  • 55. Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization.
    Zielinski B, Gratias S, Toedt G, Mendrzyk F, Stange DE, Radlwimmer B, Lohmann DR, Lichter P.
    Genes Chromosomes Cancer; 2005 Jul 01; 43(3):294-301. PubMed ID: 15834944
    [Abstract] [Full Text] [Related]

  • 56. Partial monosomy 22pter leads to q11 in a newborn with the clinical features of trisomy 13 syndrome.
    Back E, Stier R, Böhm N, Adlung A, Hameister H.
    Ann Genet; 1980 Jul 01; 23(4):244-8. PubMed ID: 6971606
    [Abstract] [Full Text] [Related]

  • 57. [Human chromosome polymorphism and disordered reproductive function. II. C-variant chromosomes].
    Tsvetkova TG, Iankova MF.
    Genetika; 1979 Jul 01; 15(10):1870-9. PubMed ID: 91543
    [Abstract] [Full Text] [Related]

  • 58. Homogeneously staining regions and tumorigenicity.
    Gilbert F, Balaban G, Brangman D, Herrmann N, Lister A.
    Int J Cancer; 1983 Jun 15; 31(6):765-8. PubMed ID: 6862685
    [Abstract] [Full Text] [Related]

  • 59. Autosomal mendelian disorders and microcytogenetics.
    de Grouchy J, Turleau C.
    Recenti Prog Med; 1990 May 15; 81(5):337-43. PubMed ID: 2198645
    [Abstract] [Full Text] [Related]

  • 60. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
    Hegmann KM, Spikes AS, Orr-Urtreger A, Shaffer LG.
    Am J Med Genet; 1996 Jan 02; 61(1):10-5. PubMed ID: 8741910
    [Abstract] [Full Text] [Related]

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