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2. [Increased sister-chromatid exchanges in fibroblasts from a del(13)-retinoblastoma patient (author's transl)]. Turleau C, Cabanis MO, de Grouchy J. Ann Genet; 1980; 23(3):169-70. PubMed ID: 6968533 [Abstract] [Full Text] [Related]
4. Sister chromatid exchanges and chromosome aberrations in fibroblasts from patients with retinoblastoma. Takabayashi T, Lin MS, Wilson MG. Hum Genet; 1983; 63(4):317-9. PubMed ID: 6862435 [Abstract] [Full Text] [Related]
6. Bilateral retinoblastoma associated with 13q-mosaicism. Possible manifestation of a germinal mutation. Ribeiro MC, Andrade JA, Erwenne CM, Brunoni D. Cancer Genet Cytogenet; 1988 Jun; 32(2):169-75. PubMed ID: 3365680 [Abstract] [Full Text] [Related]
7. Lymphocyte chromosome survey in 42 patients with retinoblastoma: effort to detect 13q14 deletion mosaicism. Motegi T. Hum Genet; 1981 Jun; 58(2):168-73. PubMed ID: 7287000 [Abstract] [Full Text] [Related]
10. Analysis of spontaneous, carcinogen-induced and promoter-induced chromosomal instability in patients with hereditary retinoblastoma. Gainer HS, Kinsella AR. Int J Cancer; 1983 Oct 15; 32(4):449-53. PubMed ID: 6618708 [Abstract] [Full Text] [Related]
11. Frequency of 13q abnormalities among 203 patients with retinoblastoma. Bunin GR, Emanuel BS, Meadows AT, Buckley JD, Woods WG, Hammond GD. J Natl Cancer Inst; 1989 Mar 01; 81(5):370-4. PubMed ID: 2915374 [Abstract] [Full Text] [Related]
12. Sister chromatid exchanges in patients with retinoblastoma. Der-Sarkissian H, Bonaïti-Pellié, Briard-Guillemot ML, Zucker JM. Cancer Genet Cytogenet; 1982 Sep 01; 7(1):73-7. PubMed ID: 7139595 [Abstract] [Full Text] [Related]
13. [Studies on deletions on chromosome 13 and their transmission in patients with retinoblastoma]. Gao Y. Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1991 Jun 01; 13(3):157-60. PubMed ID: 1831719 [Abstract] [Full Text] [Related]
15. Genetic predisposition to retinoblastoma (Rb). Zheng Y, Tang D, Peng H. Yan Ke Xue Bao; 1993 Sep 01; 9(3):149-52, 125. PubMed ID: 8168611 [No Abstract] [Full Text] [Related]
16. 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 01; 24(11):696-7. PubMed ID: 3430545 [Abstract] [Full Text] [Related]
17. High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods). Motegi T. Hum Genet; 1982 Nov 01; 61(2):95-7. PubMed ID: 7129450 [No Abstract] [Full Text] [Related]
18. 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 01; 27(1):27-31. PubMed ID: 3472646 [Abstract] [Full Text] [Related]
19. [Sister chromatid exchange (SCE) in lymphocytes of patients with cancer of the cervix uteri]. Yokota K, Ueda K, Takenaka M, Fujiwara A, Ohama K. Nihon Sanka Fujinka Gakkai Zasshi; 1987 Feb 01; 39(2):249-55. PubMed ID: 3102651 [Abstract] [Full Text] [Related]
20. Incidence and significance of a deletion of chromosome band 13q14 in patients with retinoblastoma and in their families. Liberfarb RM, Bustos T, Miller WA, Sang D. Ophthalmology; 1984 Dec 01; 91(12):1695-9. PubMed ID: 6521998 [Abstract] [Full Text] [Related] Page: [Next] [New Search]