188 related articles for article (PubMed ID: 7666401)
1. Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastoma.
Szijan I; Lohmann DR; Parma DL; Brandt B; Horsthemke B
J Med Genet; 1995 Jun; 32(6):475-9. PubMed ID: 7666401
[TBL] [Abstract][Full Text] [Related]
2. Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation.
Brichard B; Heusterspreute M; De Potter P; Chantrain C; Vermylen C; Sibille C; Gala JL
Eur J Cancer; 2006 Jan; 42(1):65-72. PubMed ID: 16343894
[TBL] [Abstract][Full Text] [Related]
3. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
Serrano ML; Yunis JJ
Biomedica; 2013; 33(1):53-61. PubMed ID: 23715307
[TBL] [Abstract][Full Text] [Related]
4. RB1 germ-line deletions in Argentine retinoblastoma patients.
Fernández C; Repetto K; Dalamon V; Bergonzi F; Ferreiro V; Szijan I
Mol Diagn Ther; 2007; 11(1):55-61. PubMed ID: 17286450
[TBL] [Abstract][Full Text] [Related]
5. Spectrum of RB1 mutations in argentine patients: 20-years experience in the molecular diagnosis of retinoblastoma.
Ottaviani D; Parma D; Giliberto F; Ferrer M; Fandino A; Davila MT; Chantada G; Szijan I
Ophthalmic Genet; 2013 Dec; 34(4):189-98. PubMed ID: 23301675
[TBL] [Abstract][Full Text] [Related]
6. Identification of germline mutations in the RB1 gene by denaturant gradient gel electrophoresis and polymerase chain reaction direct sequencing.
Blanquet V; Turleau C; Gross MS; Goossens M; Besmond C
Hum Mol Genet; 1993 Jul; 2(7):975-9. PubMed ID: 8364580
[TBL] [Abstract][Full Text] [Related]
7. Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing.
Hogg A; Onadim Z; Baird PN; Cowell JK
Oncogene; 1992 Jul; 7(7):1445-51. PubMed ID: 1352398
[TBL] [Abstract][Full Text] [Related]
8. Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma.
Blanquet V; Turleau C; Gross-Morand MS; Sénamaud-Beaufort C; Doz F; Besmond C
Hum Mol Genet; 1995 Mar; 4(3):383-8. PubMed ID: 7795591
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Detection of mutations of the RB1 gene in retinoblastoma patients by using exon-by-exon PCR-SSCP analysis.
Shimizu T; Toguchida J; Kato MV; Kaneko A; Ishizaki K; Sasaki MS
Am J Hum Genet; 1994 May; 54(5):793-800. PubMed ID: 8178820
[TBL] [Abstract][Full Text] [Related]
11. Frequency and nature of germline Rb-1 gene mutations in a series of patients with sporadic unilateral retinoblastoma.
Zajaczek S; Jakubowska A; Górski B; Kurzawski G; Krzystolik Z; Lubiński J
Eur J Cancer; 1999 Dec; 35(13):1824-7. PubMed ID: 10673998
[TBL] [Abstract][Full Text] [Related]
12. Two independent RB1-inactivating mutations in peripheral blood DNA of a hereditary retinoblastoma patient.
Alonso J; Menéndez I; López A; Frayle H; Ruisánchez N; Pestaña A
Genes Chromosomes Cancer; 2004 Jul; 40(3):271-5. PubMed ID: 15139006
[TBL] [Abstract][Full Text] [Related]
13. Enhanced sensitivity for detection of low-level germline mosaic RB1 mutations in sporadic retinoblastoma cases using deep semiconductor sequencing.
Chen Z; Moran K; Richards-Yutz J; Toorens E; Gerhart D; Ganguly T; Shields CL; Ganguly A
Hum Mutat; 2014 Mar; 35(3):384-91. PubMed ID: 24282159
[TBL] [Abstract][Full Text] [Related]
14. Rapid identification of germline mutations in retinoblastoma by protein truncation testing.
Tsai T; Fulton L; Smith BJ; Mueller RL; Gonzalez GA; Uusitalo MS; O'Brien JM
Arch Ophthalmol; 2004 Feb; 122(2):239-48. PubMed ID: 14769601
[TBL] [Abstract][Full Text] [Related]
15. Detection of germline mutations in argentine retinoblastoma patients: low and full penetrance retinoblastoma caused by the same germline truncating mutation.
Dalamón V; Surace E; Giliberto F; Ferreiro V; Fernandez C; Szijan I
J Biochem Mol Biol; 2004 Mar; 37(2):246-53. PubMed ID: 15469703
[TBL] [Abstract][Full Text] [Related]
16. The spectrum of RB1 germ-line mutations in hereditary retinoblastoma.
Lohmann DR; Brandt B; Höpping W; Passarge E; Horsthemke B
Am J Hum Genet; 1996 May; 58(5):940-9. PubMed ID: 8651278
[TBL] [Abstract][Full Text] [Related]
17. Detection of RB germline mutations using exon-by-exon heteroduplex analysis compared with SSCP.
Zhang Q; Minoda K
Yan Ke Xue Bao; 1996 Sep; 12(3):151-7. PubMed ID: 9639842
[TBL] [Abstract][Full Text] [Related]
18. Genetic testing in Tunisian families with heritable retinoblastoma using a low cost approach permits accurate risk prediction in relatives and reveals incomplete penetrance in adults.
Ayari Jeridi H; Bouguila H; Ansperger-Rescher B; Baroudi O; Mdimegh I; Omran I; Charradi K; Bouzayene H; Benammar-Elgaaïed A; Lohmann DR
Exp Eye Res; 2014 Jul; 124():48-55. PubMed ID: 24810223
[TBL] [Abstract][Full Text] [Related]
19. Exon-by-exon screening for RB germline mutations using Heteroduplex-SSCP analysis.
Zhang Q; Minoda K; Zeng R; Wu Z; Xiao X; Li S; Zhang F
Yan Ke Xue Bao; 1997 Mar; 13(1):5-11. PubMed ID: 11189328
[TBL] [Abstract][Full Text] [Related]
20. Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications.
Alonso J; García-Miguel P; Abelairas J; Mendiola M; Sarret E; Vendrell MT; Navajas A; Pestaña A
Hum Mutat; 2001 May; 17(5):412-22. PubMed ID: 11317357
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]