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Journal Abstract Search

138 related items for PubMed ID: 8689618

  • 41. Molecular diagnosis in patients with retinoblastoma: Report of a series of cases.
    Ossandón D, Zanolli M, López JP, Benavides F, Pérez V, Repetto GM.
    Arch Soc Esp Oftalmol; 2016 Aug; 91(8):379-84. PubMed ID: 27021801
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  • 45. Retinoblastoma: a prototypic hereditary neoplasm.
    Knudson AG.
    Semin Oncol; 1978 Mar; 5(1):57-60. PubMed ID: 635597
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  • 46. Nonrandom chromosomal changes in retinoblastomas.
    Pogosianz HE, Kuznetsova LE.
    Arch Geschwulstforsch; 1986 Mar; 56(2):135-43. PubMed ID: 3707294
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  • 47. [Retinoblastoma and interstitial deletion of 13q (author's transl)].
    De Grouchy J, Turleau C, Cabanis MO, Richardet JM.
    Arch Fr Pediatr; 1980 Oct; 37(8):531-5. PubMed ID: 7447607
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  • 48. Translocation X;13 in a patient with retinoblastoma.
    Ponzio G, Savin E, Cattaneo G, Ghiotti MP, Marra A, Zuffardi O, Danesino C.
    J Med Genet; 1987 Jul; 24(7):431-4. PubMed ID: 3612720
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  • 49. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production.
    Ogino W, Takeshima Y, Nishiyama A, Yagi M, Oka N, Matsuo M.
    Kobe J Med Sci; 2007 Jul; 53(4):143-50. PubMed ID: 17932453
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  • 50. 47,XY,+der(X)t(X;18)(p11.4;p11.22): A Unique Aneuploidy Associated with Klinefelter Syndrome due to an Extra Derivative X Chromosome Inherited Maternally.
    Liang J, Zhang Y, Wang R, Liang Z, Yue J, Liu R.
    Cytogenet Genome Res; 2015 Jul; 146(3):204-10. PubMed ID: 26430900
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  • 51. Characterization by FISH of a t(5;13) in a patient with bilateral retinoblastoma.
    Triviño E, Guitart M, Egozcue J, Coll MD.
    Cancer Genet Cytogenet; 1997 Jul 01; 96(1):23-5. PubMed ID: 9209465
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  • 54. Bleomycin-induced chromosome breakage in G2 lymphocytes of retinoblastoma patients.
    Chaum E, Doucette LA, Ellsworth RM, Abramson DH, Haik BG, Kitchin FD, Chaganti RS.
    Cytogenet Cell Genet; 1984 Jul 01; 38(2):152-4. PubMed ID: 6205825
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  • 56. Radiographic findings in 13q-syndrome.
    Kaste SC, Pratt CB.
    Pediatr Radiol; 1993 Jul 01; 23(7):545-8. PubMed ID: 8309761
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  • 57. Chromosomal abnormalities in human retinoblastoma. A review.
    Potluri VR, Helson L, Ellsworth RM, Reid T, Gilbert F.
    Cancer; 1986 Aug 01; 58(3):663-71. PubMed ID: 3524791
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  • 58. Chromosome evolution and high-resolution analysis of leucocytes, bone marrow, and tumor cells of retinoblastoma patients.
    Lemieux N, Richer CL.
    Am J Med Genet; 1990 Aug 01; 36(4):456-62. PubMed ID: 2389803
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  • 59. Genetic counseling in a patient with XXY/XXXY/XY mosaic Klinefelter's syndrome: estimate of sex chromosome aberrations in sperm before intracytoplasmic sperm injection.
    Kruse R, Guttenbach M, Schartmann B, Schubert R, van der Ven H, Schmid M, Propping P.
    Fertil Steril; 1998 Mar 01; 69(3):482-5. PubMed ID: 9531882
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