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Journal Abstract Search

128 related items for PubMed ID: 4054790

  • 61. Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D.
    Rivera H, Turleau C, de Grouchy J, Junien C, Despoisse S, Zucker JM.
    Hum Genet; 1981; 59(3):211-4. PubMed ID: 7327583
    [Abstract] [Full Text] [Related]

  • 62. A case of retinoblastoma, associated with histiocytosis-X and mosaicism of a deleted D-group chromosome (13q14 leads to q31).
    Orye E, Benoit Y, Coppieters R, Jeannin P, Vercruysse C, Delaey J, Delbeke MJ.
    Clin Genet; 1982 Jul; 22(1):37-9. PubMed ID: 6983401
    [No Abstract] [Full Text] [Related]

  • 63. Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma.
    Cowell JK, Rutland P, Hungerford J, Jay M.
    Hum Genet; 1988 Sep; 80(1):43-5. PubMed ID: 2901396
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  • 64. Dedicated ophthalmic research.
    Anderson B.
    N C Med J; 1991 Jan; 52(1):33-4. PubMed ID: 1996146
    [No Abstract] [Full Text] [Related]

  • 65. [Bilateral retinal malignant tumor complicating coloboma and associated with karyotype changes].
    Woillez M, Dascotte JC, Cousin P.
    Bull Soc Ophtalmol Fr; 1977 Apr; 77(4):545-6. PubMed ID: 608264
    [No Abstract] [Full Text] [Related]

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  • 71. Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosis.
    Junien C, Despoisse S, Turleau C, Nicolas H, Picard F, Le Marec B, Kaplan JC, de Grouchy J.
    Cancer Genet Cytogenet; 1982 Aug; 6(4):281-7. PubMed ID: 7116321
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  • 72. [Genetic aspects of retinoblastoma].
    Walbaum R.
    Bull Soc Ophtalmol Fr; 1977 Apr; 77(4):533-6. PubMed ID: 608260
    [No Abstract] [Full Text] [Related]

  • 73. D-group deletion syndromes and retinoblastoma.
    O'Grady RB, Rothstein TB, Romano PE.
    Am J Ophthalmol; 1974 Jan; 77(1):40-5. PubMed ID: 4824172
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  • 75. Detection by electron microscopy of a small subband 13q14.11 deletion in an hereditary retinoblastoma.
    Lemieux N, Messier PE, Drouin R, Jacob JL, Milot J, Richer CL.
    Cancer Genet Cytogenet; 1990 Sep; 48(2):265-9. PubMed ID: 2397457
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  • 76. Further observations on a 13qXp translocation associated with retinoblastoma.
    Nichols WW, Miller RC, Sobel M, Hoffman E, Sparkes RS, Mohandas T, Veomett I, Davis JR.
    Am J Ophthalmol; 1980 May; 89(5):621-7. PubMed ID: 7189644
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  • 77. An unusual family with retinoblastoma.
    Sabbah R, Berry FD, Schimmelpfennig W.
    Ann Ophthalmol; 1981 May; 13(5):595-6. PubMed ID: 7258954
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  • 78. [Role of genetic disorders in the development of retinoblastoma].
    Sporny S, Pruszczyński M.
    Pol Tyg Lek; 1979 Jan 15; 34(3):107-9. PubMed ID: 424339
    [No Abstract] [Full Text] [Related]

  • 79. X-ray, UV and chemical mutagen sensitivities of skin fibroblasts from patients with familial and chromosome 13q- retinoblastomas.
    Fujiwara Y, Miyazaki N, Kano Y, Takahashi T, Kaneko A.
    J Radiat Res; 1981 Dec 15; 22(4):472-6. PubMed ID: 7338842
    [No Abstract] [Full Text] [Related]

  • 80. The significance of genetic research in ophthalmology.
    Francois J.
    Birth Defects Orig Artic Ser; 1982 Dec 15; 18(6):3-25. PubMed ID: 6293603
    [No Abstract] [Full Text] [Related]

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