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Journal Abstract Search
125 related items for PubMed ID: 6885063
21. 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]
23. [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 [Abstract] [Full Text] [Related]
24. Chromosome 13 deletion syndrome: report of a new case and discussion of the different etiologic patterns of retinoblastoma. Lungarotti MS, Mariotti G, Quarta C, Delogu A, Fiore C. Ophthalmologica; 1980 Oct 31; 181(5):245-50. PubMed ID: 7243183 [Abstract] [Full Text] [Related]
25. Recent studies of the retinoblastoma gene. What it means to the ophthalmologist. Albert DM, Dryja TP. Arch Ophthalmol; 1988 Feb 31; 106(2):181-2. PubMed ID: 3422555 [No Abstract] [Full Text] [Related]
27. Retinoblastoma and esterase D. Mueller RF. Lancet; 1982 Oct 09; 2(8302):823. PubMed ID: 6126695 [No Abstract] [Full Text] [Related]
28. Retinoblastoma, gross internal malformations, and deletion 13q14 leads to q31. Yunis E, Zuñiga R, Ramírez E. Hum Genet; 1981 Oct 09; 56(3):283-6. PubMed ID: 7239512 [No Abstract] [Full Text] [Related]
29. Low incidence of deletion of the esterase D locus in retinoblastoma patients. Dryja TP, Bruns GA, Gallie B, Petersen R, Green W, Rapaport JM, Albert DM, Gerald PS. Hum Genet; 1983 Oct 09; 64(2):151-5. PubMed ID: 6885050 [Abstract] [Full Text] [Related]
30. Cytogenetics in retinoblastomas. Rao KS, Rao CR, Radhakrishna G. Indian J Ophthalmol; 1975 Oct 09; 23(3):23-5. PubMed ID: 1236311 [No Abstract] [Full Text] [Related]
31. Lymphocyte chromosome survey in 42 patients with retinoblastoma: effort to detect 13q14 deletion mosaicism. Motegi T. Hum Genet; 1981 Oct 09; 58(2):168-73. PubMed ID: 7287000 [Abstract] [Full Text] [Related]
32. High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods). Motegi T. Hum Genet; 1982 Oct 09; 61(2):95-7. PubMed ID: 7129450 [No Abstract] [Full Text] [Related]
33. Clues from familial cancer. Lancet; 1984 Jun 02; 1(8388):1219-20. PubMed ID: 6144930 [No Abstract] [Full Text] [Related]
34. Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas. Riccardi VM, Hittner HM, Francke U, Pippin S, Holmquist GP, Kretzer FL, Ferrell R. Clin Genet; 1979 Apr 02; 15(4):332-45. PubMed ID: 436330 [Abstract] [Full Text] [Related]
36. Oncogenesis of retinoblastoma. Verma RS, Kopelowitz N. Ann Ophthalmol; 1985 Nov 02; 17(11):701-3. PubMed ID: 4083659 [No Abstract] [Full Text] [Related]
37. Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D. Rivera H, Turleau C, de Grouchy J, Junien C, Despoisse S, Zucker JM. Hum Genet; 1981 Nov 02; 59(3):211-4. PubMed ID: 7327583 [Abstract] [Full Text] [Related]
38. Retinoblastoma, chromosome 13, and in vitro cellular radiosensitivity. Nove J, Little JB, Weichselbaum RR, Nichols WW, Hoffman E. Cytogenet Cell Genet; 1979 Nov 02; 24(3):176-84. PubMed ID: 477414 [Abstract] [Full Text] [Related]
39. Esterase D and hereditary retinoblastoma. Burde RM. Am J Ophthalmol; 1984 Jun 02; 97(6):779-82. PubMed ID: 6731544 [No Abstract] [Full Text] [Related]
40. 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 02; 32(2):169-75. PubMed ID: 3365680 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]