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Journal Abstract Search

217 related items for PubMed ID: 3391612

  • 1. Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients.
    Ejima Y, Sasaki MS, Kaneko A, Tanooka H.
    Hum Genet; 1988 Jun; 79(2):118-23. PubMed ID: 3391612
    [Abstract] [Full Text] [Related]

  • 2. Cytogenetic analysis of retinoblastoma: evidence for multifocal origin and in vivo gene amplification.
    Chaum E, Ellsworth RM, Abramson DH, Haik BG, Kitchin FD, Chaganti RS.
    Cytogenet Cell Genet; 1984 Jun; 38(2):82-91. PubMed ID: 6467991
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  • 3. Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes.
    Balaban G, Gilbert F, Nichols W, Meadows AT, Shields J.
    Cancer Genet Cytogenet; 1982 Jul; 6(3):213-21. PubMed ID: 7116319
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  • 4. First cytogenetic evidence of homozygosity for the retinoblastoma deletion in chromosome 13.
    Lemieux N, Milot J, Barsoum-Homsy M, Michaud J, Leung TK, Richer CL.
    Cancer Genet Cytogenet; 1989 Nov; 43(1):73-8. PubMed ID: 2790775
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  • 5. De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.
    Calzolari E, Palazzi P, Aiello V, Mazzeo E, Perri P, Minelli A, del Senno L, Patracchini P, Bernardi F.
    Hum Genet; 1987 Sep; 77(1):51-4. PubMed ID: 3502696
    [Abstract] [Full Text] [Related]

  • 6. Bilateral retinoblastoma associated with 13q-mosaicism. Possible manifestation of a germinal mutation.
    Ribeiro MC, Andrade JA, Erwenne CM, Brunoni D.
    Cancer Genet Cytogenet; 1988 Jun; 32(2):169-75. PubMed ID: 3365680
    [Abstract] [Full Text] [Related]

  • 7. Frequency of 13q abnormalities among 203 patients with retinoblastoma.
    Bunin GR, Emanuel BS, Meadows AT, Buckley JD, Woods WG, Hammond GD.
    J Natl Cancer Inst; 1989 Mar 01; 81(5):370-4. PubMed ID: 2915374
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  • 8. [Hereditary tumors and chromosome aberrations with special reference to retinoblastoma].
    Sasaki MS.
    Gan To Kagaku Ryoho; 1986 Mar 01; 13(3 Pt 2):645-51. PubMed ID: 3963835
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  • 10. Chromosomal anomalies in patients with retinoblastoma.
    Wilson MG, Ebbin AJ, Towner JW, Spencer WH.
    Clin Genet; 1977 Jul 01; 12(1):1-8. PubMed ID: 891004
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  • 14. [A chromosomal study on the retinoblastoma solid tumor].
    Ou BX.
    Zhonghua Yan Ke Za Zhi; 1988 May 01; 24(3):155-9. PubMed ID: 3147866
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  • 17. Diagnosis of retinoblastoma in a presymptomatic stage after detection of interstitial chromosomal deletion 13q.
    Kennerknecht I, Barbi G, Greher J.
    Ophthalmic Genet; 1994 Mar 01; 15(1):19-24. PubMed ID: 7953248
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  • 18. 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
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  • 19. Constitutional karyotypes in retinoblastoma.
    Turleau C, De Grouchy J.
    Ophthalmic Paediatr Genet; 1987 Mar 01; 8(1):11-7. PubMed ID: 3295639
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