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PUBMED FOR HANDHELDS

Journal Abstract Search


125 related items for PubMed ID: 3561603

  • 21. [Cytogenetic studies of certain retinoblastomas].
    Mihail S, Lungeanu A.
    Arch Ophtalmol Rev Gen Ophtalmol; 1974 Nov; 34(11):801-14. PubMed ID: 4282458
    [No Abstract] [Full Text] [Related]

  • 22. Dynamic investigation on chromosome aberration of a human retinoblastoma cell line So-Rb50.
    Qu B, Zhuo Z, Yi Y, Feng G, Zheng J, Liang Q, Li Y.
    Yan Ke Xue Bao; 1993 Mar; 9(1):38-9, 37. PubMed ID: 8253183
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  • 23. Chromosome errors in retinoblastoma.
    Howard RO.
    Birth Defects Orig Artic Ser; 1982 Mar; 18(6):703-27. PubMed ID: 6756503
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  • 27. Retinoblastoma and chromosome 13 deletion.
    Gencík A, Auf der Maur P, Gencíkova A, Lütschg J.
    Helv Paediatr Acta; 1982 Mar; 37(5):457-64. PubMed ID: 7161117
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  • 30. Chromosome fragility in patients with sporadic unilateral retinoblastoma.
    de Nuñez M, Penchaszadeh VB, Pimentel E.
    Cancer Genet Cytogenet; 1984 Feb; 11(2):139-41. PubMed ID: 6692335
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  • 35. 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; 21(6):357-61. PubMed ID: 7127878
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  • 36. [Increased sister-chromatid exchanges in fibroblasts from a del(13)-retinoblastoma patient (author's transl)].
    Turleau C, Cabanis MO, de Grouchy J.
    Ann Genet; 1980 Jun; 23(3):169-70. PubMed ID: 6968533
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  • 37. Retinoblastoma and chromosome 13.
    Francke U.
    Birth Defects Orig Artic Ser; 1976 Jun; 12(7):131-4. PubMed ID: 1024606
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  • 38. Segregation of chromosome 13 in retinoblastoma.
    Knight LA, Gardner HA, Gallie BL.
    Lancet; 1978 May 06; 1(8071):989. PubMed ID: 76915
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  • 39. Retinoblastoma. A model of hereditary fragile chromosomal regions.
    Hashem N, Khalifa S.
    Hum Hered; 1975 May 06; 25(1):35-49. PubMed ID: 1150293
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