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Journal Abstract Search

149 related items for PubMed ID: 2206862

  • 21. Diagnosis of retinoblastoma in a presymptomatic stage after detection of interstitial chromosomal deletion 13q.
    Kennerknecht I, Barbi G, Greher J.
    Ophthalmic Genet; 1994 Mar; 15(1):19-24. PubMed ID: 7953248
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  • 22. Recent developments in the genetics and treatment of retinoblastoma.
    Murphree AL, Gomer CJ, Doiron DR, Benedict WF.
    Birth Defects Orig Artic Ser; 1982 Mar; 18(6):681-7. PubMed ID: 7171784
    [No Abstract] [Full Text] [Related]

  • 23. Retinoblastoma--genetic insights into neoplasia.
    Nyhan WL.
    Bioessays; 1987 Jan; 6(1):5-8. PubMed ID: 2882750
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  • 24. Esterase D assay in Brazilian retinoblastoma families.
    Costanzi E, da Silva-Fernandes ME, D'Almeida V, Erwenne CM.
    Am J Med Genet; 1989 Nov; 34(3):391-6. PubMed ID: 2596526
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  • 31. Association of autism, retinoblastoma, and reduced esterase D activity.
    Ritvo ER, Mason-Brothers A, Menkes JH, Sparkes RS.
    Arch Gen Psychiatry; 1988 Jun; 45(6):600. PubMed ID: 3377648
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  • 32. Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locus.
    Horsthemke B, Barnert HJ, Greger V, Passarge E, Höpping W.
    Lancet; 1987 Feb 28; 1(8531):511-2. PubMed ID: 2881072
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  • 33. The genetics of retinoblastoma.
    Sparkes RS.
    Biochim Biophys Acta; 1985 Feb 28; 780(2):95-118. PubMed ID: 3890943
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  • 34. Effect of the esterase-D phenotype on its in vitro enzyme activity.
    Cowell JK, Rutland P, Jay M, Hungerford J.
    Hum Genet; 1986 Nov 28; 74(3):298-301. PubMed ID: 3465678
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  • 36. 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 Nov 28; 32(3):144-8. PubMed ID: 2554783
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