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24. Deletion in one allele and a rare neutral DNA alteration in the other allele of the RB1 gene in a patient with bilateral retinoblastoma. Horsthemke B; Brandt B; Albrecht B; Passarge E Am J Med Genet; 1992 Sep; 44(2):255. PubMed ID: 1456305 [No Abstract] [Full Text] [Related]
25. Multiple manifestations of the retinoblastoma gene. Gallie BL; Phillips RA Birth Defects Orig Artic Ser; 1982; 18(6):689-701. PubMed ID: 7171785 [No Abstract] [Full Text] [Related]
26. Recent developments in the genetics and treatment of retinoblastoma. Murphree AL; Gomer CJ; Doiron DR; Benedict WF Birth Defects Orig Artic Ser; 1982; 18(6):681-7. PubMed ID: 7171784 [No Abstract] [Full Text] [Related]
27. Expression and amplification of the N-myc gene in primary retinoblastoma. Lee WH; Murphree AL; Benedict WF Nature; 1984 May 31-Jun 6; 309(5967):458-60. PubMed ID: 6728001 [TBL] [Abstract][Full Text] [Related]
30. Contribution and mechanisms of genetic predisposition to cancer: hereditary cancers and anti-oncogenes. Knudson AG Prog Clin Biol Res; 1983; 132C():351-60. PubMed ID: 6314359 [No Abstract] [Full Text] [Related]
31. Multiple changes in oncogenes and tumor suppressor genes in human retinoblastoma. Howard RO Trans Am Ophthalmol Soc; 1996; 94():299-312; discussion 312-4. PubMed ID: 8981702 [TBL] [Abstract][Full Text] [Related]
32. 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; 36(4):456-62. PubMed ID: 2389803 [TBL] [Abstract][Full Text] [Related]
33. Mutation detection and genetic counseling in retinoblastoma using heteroduplex analysis. Zhang Q; Minoda K Jpn J Ophthalmol; 1995; 39(4):432-7. PubMed ID: 8926652 [TBL] [Abstract][Full Text] [Related]
34. Oncogenes and tumor suppressor genes. Liu E; Weissman B Cancer Treat Res; 1992; 63():1-13. PubMed ID: 1363351 [No Abstract] [Full Text] [Related]
35. Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma. Greger V; Kerst S; Messmer E; Höpping W; Passarge E; Horsthemke B J Med Genet; 1988 Apr; 25(4):217-21. PubMed ID: 3163379 [TBL] [Abstract][Full Text] [Related]
37. 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 [TBL] [Abstract][Full Text] [Related]
38. Esterase D and hereditary retinoblastoma. Burde RM Am J Ophthalmol; 1984 Jun; 97(6):779-82. PubMed ID: 6731544 [No Abstract] [Full Text] [Related]
39. Recessive mutations in cancer predisposition and progression. Cavenee WK Basic Life Sci; 1991; 57():171-80; discussion 180-1. PubMed ID: 1667571 [No Abstract] [Full Text] [Related]
40. [Role of genetic disorders in the development of retinoblastoma]. Sporny S; Pruszczyński M Pol Tyg Lek; 1979 Jan; 34(3):107-9. PubMed ID: 424339 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]