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Journal Abstract Search

530 related items for PubMed ID: 3707294

  • 21. [Hereditary tumors and chromosome aberrations with special reference to retinoblastoma].
    Sasaki MS.
    Gan To Kagaku Ryoho; 1986 Mar; 13(3 Pt 2):645-51. PubMed ID: 3963835
    [Abstract] [Full Text] [Related]

  • 22. Complete or partial homozygosity of chromosome 13 in primary retinoblastoma.
    Benedict WF, Srivatsan ES, Mark C, Banerjee A, Sparkes RS, Murphree AL.
    Cancer Res; 1987 Aug 01; 47(15):4189-91. PubMed ID: 2886215
    [Abstract] [Full Text] [Related]

  • 23. Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses.
    Mairal A, Pinglier E, Gilbert E, Peter M, Validire P, Desjardins L, Doz F, Aurias A, Couturier J.
    Genes Chromosomes Cancer; 2000 Aug 01; 28(4):370-9. PubMed ID: 10862045
    [Abstract] [Full Text] [Related]

  • 24. Genetics of embryonal tumours of childhood: retinoblastoma, Wilms' tumour and neuroblastoma.
    Brodeur GM.
    Cancer Surv; 1995 Aug 01; 25():67-99. PubMed ID: 8718513
    [Abstract] [Full Text] [Related]

  • 25. [Retinoblastoma and transmission of balanced chromosomal modifications].
    Bec P, Arne JL, Bourrouillou G, Colombies P.
    Mod Probl Ophthalmol; 1977 Aug 01; 18():160-4. PubMed ID: 876047
    [Abstract] [Full Text] [Related]

  • 26. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
    Grammatico P, Majore S, Marrocco G, Poscente M, Mordenti C, Grammatico B, Del Porto G.
    Genet Couns; 1999 Aug 01; 10(4):351-8. PubMed ID: 10631922
    [Abstract] [Full Text] [Related]

  • 27. Nonrandom chromosomal changes in untreated retinoblastomas.
    Benedict WF, Banerjee A, Mark C, Murphree AL.
    Cancer Genet Cytogenet; 1983 Dec 01; 10(4):311-33. PubMed ID: 6652613
    [Abstract] [Full Text] [Related]

  • 28. [Karyotyping in chronic myeloproliferative syndrome (except chronic myeloid leukemia)].
    Lessard M.
    Pathol Biol (Paris); 1982 Nov 01; 30(9):759-65. PubMed ID: 6760079
    [Abstract] [Full Text] [Related]

  • 29. [RV polymorphism of the chromosomes in newborn infants].
    Krachunova M, Tsancheva M, Lozanova T.
    Eksp Med Morfol; 1980 Nov 01; 19(3):144-8. PubMed ID: 7418645
    [Abstract] [Full Text] [Related]

  • 30. 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
    [Abstract] [Full Text] [Related]

  • 31. Autosomal chromosome aberrations in ophthalmology.
    Francois J.
    Int Ophthalmol Clin; 1968 Jul 01; 8(4):839-910. PubMed ID: 4244691
    [No Abstract] [Full Text] [Related]

  • 32. Cytogenetics of heritability in cancer.
    Evans HJ.
    IARC Sci Publ; 1982 Jul 01; (39):35-56. PubMed ID: 6295935
    [Abstract] [Full Text] [Related]

  • 33. Retinoblastoma, chromosome abnormalities and oncogene expression.
    Gilbert F, Potluri VR, Short MP, Kau CL, Lalatta F.
    Ophthalmic Paediatr Genet; 1987 Mar 01; 8(1):3-10. PubMed ID: 3295640
    [Abstract] [Full Text] [Related]

  • 34. Nonrandom chromosomal changes in transitional cell carcinoma of the bladder.
    Gibas Z, Prout GR, Connolly JG, Pontes JE, Sandberg AA.
    Cancer Res; 1984 Mar 01; 44(3):1257-64. PubMed ID: 6692407
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32----qter.
    Al-Awadi SA, Teebi AS, Sundareshan TS.
    Ann Genet; 1985 Mar 01; 28(3):181-4. PubMed ID: 3879154
    [Abstract] [Full Text] [Related]

  • 37. Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome.
    Lillington DM, Kingston JE, Coen PG, Price E, Hungerford J, Domizio P, Young BD, Onadim Z.
    Genes Chromosomes Cancer; 2003 Feb 01; 36(2):121-8. PubMed ID: 12508240
    [Abstract] [Full Text] [Related]

  • 38. Retinoblastoma and chromosome 13 deletion.
    Gencík A, Auf der Maur P, Gencíkova A, Lütschg J.
    Helv Paediatr Acta; 1982 Feb 01; 37(5):457-64. PubMed ID: 7161117
    [Abstract] [Full Text] [Related]

  • 39.
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