360 related articles for article (PubMed ID: 14769601)
1. 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]
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. 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]
4. 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]
5. Spectrum of germline mutations in RB1 in Chinese patients with retinoblastoma: Application of targeted next-generation sequencing.
Zou Y; Li J; Hua P; Liang T; Ji X; Zhao P
Mol Vis; 2021; 27():1-16. PubMed ID: 33456302
[TBL] [Abstract][Full Text] [Related]
6. Overview of RB gene mutations in patients with retinoblastoma. Implications for clinical genetic screening.
Harbour JW
Ophthalmology; 1998 Aug; 105(8):1442-7. PubMed ID: 9709755
[TBL] [Abstract][Full Text] [Related]
7. Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.
Nichols KE; Houseknecht MD; Godmilow L; Bunin G; Shields C; Meadows A; Ganguly A
Hum Mutat; 2005 Jun; 25(6):566-74. PubMed ID: 15884040
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Screening for RB1 mutations in tumor tissue using denaturing high performance liquid chromatography, multiplex ligation-dependent probe amplification, and loss of heterozygosity analysis.
Sellner LN; Edkins E; Smith N
Pediatr Dev Pathol; 2006; 9(1):31-7. PubMed ID: 16808635
[TBL] [Abstract][Full Text] [Related]
11. [Gene diagnosis and genetic counselling of Rb gene mutations in retinoblastoma patients and their family members].
Huang Q; Dryja TP; Yandell DW
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Apr; 15(2):65-8. PubMed ID: 9531640
[TBL] [Abstract][Full Text] [Related]
12. Spectrum of germline
Rojanaporn D; Boontawon T; Chareonsirisuthigul T; Thanapanpanich O; Attaseth T; Saengwimol D; Anurathapan U; Sujirakul T; Kaewkhaw R; Hongeng S
Mol Vis; 2018; 24():778-788. PubMed ID: 30636860
[TBL] [Abstract][Full Text] [Related]
13. Improved clinical management of retinoblastoma through gene testing.
Raizis A; Clemett R; Corbett R; McGaughran J; Evans J; George P
N Z Med J; 2002 May; 115(1154):231-4. PubMed ID: 12117173
[TBL] [Abstract][Full Text] [Related]
14. Mutational screening of germline
Nguyen HH; Nguyen HTT; Vu NP; Le QT; Pham CM; Huyen TT; Manh H; Pham HLB; Nguyen TD; Le HTT; Van Nong H
Mol Vis; 2018; 24():231-238. PubMed ID: 29568217
[TBL] [Abstract][Full Text] [Related]
15. Identification of four novel RB1 germline mutations in Korean retinoblastoma patients.
Yu YS; Kim IJ; Ku JL; Park JG
Hum Mutat; 2001 Sep; 18(3):252. PubMed ID: 11524739
[TBL] [Abstract][Full Text] [Related]
16. Spectrum of mutations in the
Kiet NC; Khuong LT; Minh DD; ; Quan NHM; Xinh PT; Trang NNC; Luan NT; Khai NM; Vu HA
Mol Vis; 2019; 25():215-221. PubMed ID: 30996590
[TBL] [Abstract][Full Text] [Related]
17.
Fang X; Chen J; Wang Y; Zhao M; Zhang X; Yang L; Ni X; Zhao J; Gallie BL
Ophthalmic Genet; 2021 Oct; 42(5):593-599. PubMed ID: 34190019
[No Abstract] [Full Text] [Related]
18. Outcomes of integrating genetics in management of patients with retinoblastoma.
Dhar SU; Chintagumpala M; Noll C; Chévez-Barrios P; Paysse EA; Plon SE
Arch Ophthalmol; 2011 Nov; 129(11):1428-34. PubMed ID: 22084214
[TBL] [Abstract][Full Text] [Related]
19. Uncommon RB1 somatic mutations in a unilateral retinoblastoma patient.
Ottaviani D; Alonso C; Szijan I
Medicina (B Aires); 2015; 75(3):137-41. PubMed ID: 26117602
[TBL] [Abstract][Full Text] [Related]
20. Splicing aberrations caused by constitutional RB1 gene mutations in retinoblastoma.
Parsam VL; Ali MJ; Honavar SG; Vemuganti GK; Kannabiran C
J Biosci; 2011 Jun; 36(2):281-7. PubMed ID: 21654082
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]