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Journal Abstract Search

138 related items for PubMed ID: 8689618

  • 61. Deletion (13)(q13q14.3) with retinoblastoma: confirmation and extension of a recognisable pattern of clinical features in retinoblastoma patients with 13q deletion.
    Motegi T, Ikeda K, Watanabe K, Yanagawa Y, Minoda K.
    J Med Genet; 1987 Nov; 24(11):696-7. PubMed ID: 3430545
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  • 62. Expression of fragile sites in patients with retinoblastoma, their parents, and unaffected siblings: a study of ten families.
    Sundareshan TS, Augustus M.
    Cancer Genet Cytogenet; 1994 Nov; 78(1):72-7. PubMed ID: 7987810
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  • 63. Similar chromosomal abnormalities in several retinoblastomas.
    Kusnetsova LE, Prigogina EL, Pogosianz HE, Belkina BM.
    Hum Genet; 1982 Nov; 61(3):201-4. PubMed ID: 7173862
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  • 64. Renal cell carcinoma with X;1 translocation in a child with Klinefelter syndrome.
    Yenamandra A, Zhou X, Trinchitella L, Susin M, Sastry S, Mehta L.
    Am J Med Genet; 1998 May 26; 77(4):281-4. PubMed ID: 9600736
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  • 65. A chromosomal breakpoint that separates the esterase D and retinoblastoma predisposition loci in a patient with del(13)(q14q31).
    Cowell JK, Hungerford J, Rutland P, Jay M.
    Cancer Genet Cytogenet; 1987 Jul 26; 27(1):27-31. PubMed ID: 3472646
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  • 66. Deletion of 13q in two patients with retinoblastoma, one probably due to 13q-mosaicism in the mother.
    Michalová K, Kloucek F, Musilová J.
    Hum Genet; 1982 Jul 26; 61(3):264-6. PubMed ID: 7173873
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  • 68. Retinoblastoma in association with the chromosome breakage syndromes Fanconi's anaemia and Bloom's syndrome: clinical and cytogenetic findings.
    Gibbons B, Scott D, Hungerford JL, Cheung KL, Harrison C, Attard-Montalto S, Evans M, Birch JM, Kingston JE.
    Clin Genet; 1995 Jun 26; 47(6):311-7. PubMed ID: 7554365
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  • 71. Cerebral germ cell tumor and XXY karyotype.
    Casalone R, Righi R, Granata P, Portentoso P, Minelli E, Meroni, Solero CL, Allegranza A.
    Cancer Genet Cytogenet; 1994 May 26; 74(1):25-9. PubMed ID: 8194043
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  • 72. Chromosomal deletion and retinoblastoma.
    Knudson AG, Meadows AT, Nichols WW, Hill R.
    N Engl J Med; 1976 Nov 11; 295(20):1120-3. PubMed ID: 980006
    [No Abstract] [Full Text] [Related]

  • 73. The genetics of retinoblastoma.
    Stahl A, Levy N, Wadzynska T, Sussan JM, Jourdan-Fonta D, Saracco JB.
    Ann Genet; 1994 Nov 11; 37(4):172-8. PubMed ID: 7710251
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  • 75. 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 11; 77(1):51-4. PubMed ID: 3502696
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  • 76. Another small supernumerary marker chromosome derived from chromosome 9 in a Klinefelter patient.
    Gulten T, Gorukmez O, Gorukmez O, Karkucak M, Ture M, Yakut T.
    West Indian Med J; 2012 Dec 11; 61(9):924-7. PubMed ID: 24020236
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  • 79. [Cytogenetics and Y chromosome AZF microdeletions in infertile patients with mosaic karyotype Klinefelter syndrome (46,XY/47,XXY/48, XXYY/49,XXXXY)].
    Tian L, Zhang JW, Shen CX, Du Y, Zhou X.
    Zhonghua Nan Ke Xue; 2012 Jun 11; 18(6):545-50. PubMed ID: 22774613
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  • 80. [2 cases of Klinefelter's syndrome with XY-XXY mosaic].
    Kunze-Mühl E, Fischer P, Eisenhut L.
    Wien Klin Wochenschr; 1965 Dec 10; 77(49):976. PubMed ID: 5870421
    [No Abstract] [Full Text] [Related]

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