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PUBMED FOR HANDHELDS

Journal Abstract Search


220 related items for PubMed ID: 2582950

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. A genetic study of retinoblastoma.
    Liu XX, Sun YJ, Zhang L.
    J Tongji Med Univ; 1991; 11(4):220-4. PubMed ID: 1819032
    [Abstract] [Full Text] [Related]

  • 3.
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  • 4. Chromosome errors in retinoblastoma.
    Howard RO.
    Birth Defects Orig Artic Ser; 1982; 18(6):703-27. PubMed ID: 6756503
    [No Abstract] [Full Text] [Related]

  • 5.
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  • 7. Homozygosity of chromosome 13 in retinoblastoma.
    Dryja TP, Cavenee W, White R, Rapaport JM, Petersen R, Albert DM, Bruns GA.
    N Engl J Med; 1984 Mar 01; 310(9):550-3. PubMed ID: 6694706
    [Abstract] [Full Text] [Related]

  • 8. Oncogenesis of retinoblastoma.
    Verma RS, Kopelowitz N.
    Ann Ophthalmol; 1985 Nov 01; 17(11):701-3. PubMed ID: 4083659
    [No Abstract] [Full Text] [Related]

  • 9. [The genetic study of retinoblastoma].
    Li AR, Fang QX, Luo CG, Xia RN, Zhou JM, Qiu JC, Li SJ, Hu SN, Wang H, Wang YP.
    Yan Ke Xue Bao; 1988 Jun 01; 4(2):73-7. PubMed ID: 3240815
    [No Abstract] [Full Text] [Related]

  • 10. The decrease of catalase or esterase D activity in patients with microdeletions of 11p or 13q does not increase their radiosensitivity.
    Sabatier L, Hoffschir F, al Achkar WA, Turleau C, de Grouchy J, Dutrillaux B.
    Ann Genet; 1989 Jun 01; 32(3):144-8. PubMed ID: 2554783
    [Abstract] [Full Text] [Related]

  • 11. The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions.
    Cowell JK, Thompson E, Rutland P.
    Arch Dis Child; 1987 Jan 01; 62(1):8-11. PubMed ID: 3813643
    [Abstract] [Full Text] [Related]

  • 12. Esterase D studies in human retinoblastoma.
    Sparkes RS, Sparkes MC.
    Isozymes Curr Top Biol Med Res; 1983 Jan 01; 11():173-82. PubMed ID: 6642986
    [No Abstract] [Full Text] [Related]

  • 13. Low incidence of deletion of the esterase D locus in retinoblastoma patients.
    Dryja TP, Bruns GA, Gallie B, Petersen R, Green W, Rapaport JM, Albert DM, Gerald PS.
    Hum Genet; 1983 Jan 01; 64(2):151-5. PubMed ID: 6885050
    [Abstract] [Full Text] [Related]

  • 14. [Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients].
    Munier F, Balmer A, von Moos C, Pescia G, Gailloud C, van Melle G, Thonney F, Gaide AC, Allaz MJ, Rutz HP.
    Klin Monbl Augenheilkd; 1991 May 01; 198(5):419-24. PubMed ID: 1886375
    [Abstract] [Full Text] [Related]

  • 15. Occurrence of unilateral retinoblastoma in three generations of a Louisiana family.
    Haik GM.
    J La State Med Soc; 1984 Sep 01; 136(9):41-4. PubMed ID: 6491648
    [No Abstract] [Full Text] [Related]

  • 16. Molecular evidence that the esterase-D gene lies proximal to the retinoblastoma susceptibility locus in chromosome region 13q14.
    Mitchell CD, Cowell JK.
    Hum Genet; 1988 Dec 01; 81(1):57-60. PubMed ID: 3198126
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 36(4):456-62. PubMed ID: 2389803
    [Abstract] [Full Text] [Related]

  • 18. A case report of a patient with retinoblastoma and chromosome 13q deletion: assignment of a new gene (gene for LCP1) on human chromosome 13.
    Kondo I, Shin K, Honmura S, Nakajima H, Yamamura E, Satoh H, Terauchi M, Usuki Y, Takita H, Hamaguchi H.
    Hum Genet; 1985 Aug 01; 71(3):263-6. PubMed ID: 3864729
    [Abstract] [Full Text] [Related]

  • 19. A chromosomal breakpoint that separates the esterase D and retinoblastoma predisposition loci in a patient with del(13)(q14q31).
    Cowell JK, Hungerford J, Rutland P, Jay M.
    Cancer Genet Cytogenet; 1987 Jul 01; 27(1):27-31. PubMed ID: 3472646
    [Abstract] [Full Text] [Related]

  • 20. [Genetics and epidemiology of retinoblastoma].
    Matsunaga E.
    Gan No Rinsho; 1987 Apr 01; 33(5 Suppl):507-13. PubMed ID: 3474431
    [Abstract] [Full Text] [Related]


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