164 related articles for article (PubMed ID: 2901396)
21. Diagnosis of retinoblastoma in a presymptomatic stage after detection of interstitial chromosomal deletion 13q.
Kennerknecht I; Barbi G; Greher J
Ophthalmic Genet; 1994 Mar; 15(1):19-24. PubMed ID: 7953248
[TBL] [Abstract][Full Text] [Related]
22. Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma.
Lalande M; Donlon T; Petersen RA; Liberfarb R; Manter S; Latt SA
Cancer Genet Cytogenet; 1986 Oct; 23(2):151-7. PubMed ID: 3756834
[TBL] [Abstract][Full Text] [Related]
23. 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; 77(1):51-4. PubMed ID: 3502696
[TBL] [Abstract][Full Text] [Related]
24. Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene.
Scheffer H; te Meerman GJ; Kruize YC; van den Berg AH; Penninga DP; Tan KE; der Kinderen DJ; Buys CH
Am J Hum Genet; 1989 Aug; 45(2):252-60. PubMed ID: 2569269
[TBL] [Abstract][Full Text] [Related]
25. Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosis.
Junien C; Despoisse S; Turleau C; Nicolas H; Picard F; Le Marec B; Kaplan JC; de Grouchy J
Cancer Genet Cytogenet; 1982 Aug; 6(4):281-7. PubMed ID: 7116321
[TBL] [Abstract][Full Text] [Related]
26. Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus.
Ward P; Packman S; Loughman W; Sparkes M; Sparkes R; McMahon A; Gregory T; Ablin A
J Med Genet; 1984 Apr; 21(2):92-5. PubMed ID: 6716423
[TBL] [Abstract][Full Text] [Related]
27. Complete or partial homozygosity of chromosome 13 in primary retinoblastoma.
Benedict WF; Srivatsan ES; Mark C; Banerjee A; Sparkes RS; Murphree AL
Cancer Res; 1987 Aug; 47(15):4189-91. PubMed ID: 2886215
[TBL] [Abstract][Full Text] [Related]
28. Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
Dryja TP; Rapaport JM; Joyce JM; Petersen RA
Proc Natl Acad Sci U S A; 1986 Oct; 83(19):7391-4. PubMed ID: 2876425
[TBL] [Abstract][Full Text] [Related]
29. Retinoblastoma: host resistance and 13q- chromosomal deletion.
Matsunaga E
Hum Genet; 1980; 56(1):53-8. PubMed ID: 7203480
[TBL] [Abstract][Full Text] [Related]
30. 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; 81(5):370-4. PubMed ID: 2915374
[TBL] [Abstract][Full Text] [Related]
31. Activity of red cell esterase D in 50 cases of retinoblastoma patients and their family members.
Fujiki K; Kuwabara Y; Nakajima A; Nishigaki I; Ikeuchi T
Ophthalmic Paediatr Genet; 1987 Mar; 8(1):19-21. PubMed ID: 3587887
[TBL] [Abstract][Full Text] [Related]
32. Constitutional karyotypes in retinoblastoma.
Turleau C; De Grouchy J
Ophthalmic Paediatr Genet; 1987 Mar; 8(1):11-7. PubMed ID: 3295639
[TBL] [Abstract][Full Text] [Related]
33. Preferential germline mutation of the paternal allele in retinoblastoma.
Zhu XP; Dunn JM; Phillips RA; Goddard AD; Paton KE; Becker A; Gallie BL
Nature; 1989 Jul; 340(6231):312-3. PubMed ID: 2568588
[TBL] [Abstract][Full Text] [Related]
34. Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes.
Haines JL; Ozelius L; St George-Hyslop P; Wexler NS; Gusella JF; Conneally PM
Genet Epidemiol; 1988; 5(6):375-80. PubMed ID: 2905314
[TBL] [Abstract][Full Text] [Related]
35. Immortalization of fibroblasts from two patients with hereditary retinoblastoma.
Banerjee A; Srivatsan E; Hashimoto T; Takahashi R; Xu HJ; Hu SX; Benedict WF
Anticancer Res; 1992; 12(5):1347-54. PubMed ID: 1359829
[TBL] [Abstract][Full Text] [Related]
36. A deleted chromosome no. 13 in human retinoblastoma cells: relevance to tumorigenesis.
Balaban-Malenbaum G; Gilbert F; Nichols WW; Hill R; Shields J; Meadows AT
Cancer Genet Cytogenet; 1981 Apr; 3(3):243-50. PubMed ID: 7284985
[TBL] [Abstract][Full Text] [Related]
37. 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; 96(1):23-5. PubMed ID: 9209465
[TBL] [Abstract][Full Text] [Related]
38. Retinoblastoma and retinoma occurring in a child with a translocation and deletion of the long arm of chromosome 13.
Keith CG; Webb GC
Arch Ophthalmol; 1985 Jul; 103(7):941-4. PubMed ID: 4015485
[TBL] [Abstract][Full Text] [Related]
39. Retinoblastoma associated with chromosomal 13q14 deletion mosaicism.
Kivelä T; Tuppurainen K; Riikonen P; Vapalahti M
Ophthalmology; 2003 Oct; 110(10):1983-8. PubMed ID: 14522775
[TBL] [Abstract][Full Text] [Related]
40. 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; 61(3):264-6. PubMed ID: 7173873
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]