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Journal Abstract Search

140 related items for PubMed ID: 7104985

  • 41. Retinoblastoma, gross internal malformations, and deletion 13q14 leads to q31.
    Yunis E, Zuñiga R, Ramírez E.
    Hum Genet; 1981; 56(3):283-6. PubMed ID: 7239512
    [No Abstract] [Full Text] [Related]

  • 42. [The 13q14 deletion syndrome].
    Lund OE, Murken JD.
    Fortschr Ophthalmol; 1985; 82(4):385-7. PubMed ID: 4054790
    [No Abstract] [Full Text] [Related]

  • 43. 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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  • 44. [Interstitial deletion of the long arms of chromosome 13].
    Molina M, Santolaya JM, Onaindía ML, Sánchez E, De Gárate J.
    An Esp Pediatr; 1982 Apr; 16(4):346-51. PubMed ID: 7125394
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  • 45. New findings in the chromosome 13 long-arm deletion syndrome and retinoblastoma.
    Weichselbaum RR, Zakov ZN, Albert DM, Friedman AH, Nove J, Little JB.
    Ophthalmology; 1979 Jun; 86(6):1191-201. PubMed ID: 118416
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  • 53. Interstital deletion of 13q associated with retinoblastoma and congenital malformations.
    Petit P, Fryns JP.
    Ann Genet; 1979 Jun; 22(2):106-7. PubMed ID: 315199
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  • 54. The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions.
    Cowell JK, Thompson E, Rutland P.
    Arch Dis Child; 1987 Jan; 62(1):8-11. PubMed ID: 3813643
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  • 57. [Genetic study of retinoblastoma].
    Sun YJ.
    Zhonghua Yan Ke Za Zhi; 1989 May; 25(3):152-5. PubMed ID: 2582950
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  • 58. Retinoblastoma. A model of hereditary fragile chromosomal regions.
    Hashem N, Khalifa S.
    Hum Hered; 1975 May; 25(1):35-49. PubMed ID: 1150293
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