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PUBMED FOR HANDHELDS

Journal Abstract Search


225 related items for PubMed ID: 424728

  • 21. A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q.
    Motegi T, Kaga M, Yanagawa Y, Kadowaki H, Watanabe K, Inoue A, Komatsu M, Minoda K.
    Hum Genet; 1983; 64(2):160-2. PubMed ID: 6885051
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  • 22. [A case of bilateral retinoblastoma in light of genetic counseling].
    Broniarczyk-Lobowa A, Augustyniak E, Suprunowicz I, Debiec-Rychterowa M.
    Klin Oczna; 1985 Apr; 87(4):167-8. PubMed ID: 4046476
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  • 25. Retinoblastoma and chromosome abnormality. Partial deletion of the long arm of chromosome 13.
    Howard RO, Breg WR, Albert DM, Lesser RL.
    Arch Ophthalmol; 1974 Dec; 92(6):490-3. PubMed ID: 4433268
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  • 28. Nonrandom chromosomal changes in retinoblastomas.
    Pogosianz HE, Kuznetsova LE.
    Arch Geschwulstforsch; 1986 Dec; 56(2):135-43. PubMed ID: 3707294
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  • 29. Retinoblastoma, chromosome abnormalities and oncogene expression.
    Gilbert F, Potluri VR, Short MP, Kau CL, Lalatta F.
    Ophthalmic Paediatr Genet; 1987 Mar; 8(1):3-10. PubMed ID: 3295640
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  • 31. In vitro radiosensitivity of fibroblasts derived from patients with retinoblastoma and abnormalities of chromosome 13.
    Weichselbaum RR, Nichols WW, Albert DM, Little JB.
    Retina; 1983 Mar; 3(2):126-30. PubMed ID: 6878899
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  • 32. Constitutional karyotype in retinoblastoma. Case report and review of literature.
    Munier F, Pescia G, Jotterand-Bellomo M, Balmer A, Gailloud C, Thonney F.
    Ophthalmic Paediatr Genet; 1989 Jun; 10(2):129-50. PubMed ID: 2674826
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  • 33. Chromosome errors in retinoblastoma.
    Howard RO.
    Birth Defects Orig Artic Ser; 1982 Jun; 18(6):703-27. PubMed ID: 6756503
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  • 34. Retinoblastoma and subband deletion of chromosome 13.
    Yunis JJ, Ramsay N.
    Am J Dis Child; 1978 Feb; 132(2):161-3. PubMed ID: 626181
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  • 35. Retinoblastoma. A model of hereditary fragile chromosomal regions.
    Hashem N, Khalifa S.
    Hum Hered; 1975 Feb; 25(1):35-49. PubMed ID: 1150293
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  • 36. [A case of bilateral retinoblastoma with monosomy 13 (q12 leads to 114) (author's transl)].
    Walbaum R, François P, Farriaux JP, Woillez M.
    Hum Genet; 1978 Oct 31; 44(2):219-26. PubMed ID: 730167
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  • 37. Retinoblastoma and its association with a deletion in chromosome #13: a survey using high-resolution chromosome techniques.
    Johnson MP, Ramsay N, Cervenka J, Wang N.
    Cancer Genet Cytogenet; 1982 May 31; 6(1):29-37. PubMed ID: 7104985
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