145 related articles for article (PubMed ID: 20059380)
1. A c.1363C>T (p.R455X) nonsense mutation of RB1 gene in a southern Chinese retinoblastoma pedigree.
Chen CY; Xu CM; Du ZF; Chen XL; Ren GL; Zhang XN
Genet Test Mol Biomarkers; 2010 Apr; 14(2):193-6. PubMed ID: 20059380
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [Characteristics of RB1 gene mutations in Chinese patients with retinoblastoma].
He MY; An Y; Li G; Qian J; Gao YJ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Oct; 30(5):509-12. PubMed ID: 24078560
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Spectrum of germ-line RB1 gene mutations in Malaysian patients with retinoblastoma.
Mohd Khalid MK; Yakob Y; Md Yasin R; Wee Teik K; Siew CG; Rahmat J; Ramasamy S; Alagaratnam J
Mol Vis; 2015; 21():1185-90. PubMed ID: 26539030
[TBL] [Abstract][Full Text] [Related]
6. Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis.
Kalsoom S; Wasim M; Afzal S; Shahzad MS; Ramzan S; Awan AR; Anjum AA; Ramzan K
Mol Vis; 2015; 21():1085-92. PubMed ID: 26396485
[TBL] [Abstract][Full Text] [Related]
7. Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.
Abidi O; Knari S; Sefri H; Charif M; Senechal A; Hamel C; Rouba H; Zaghloul K; El Kettani A; Lenaers G; Barakat A
Mol Vis; 2011; 17():3541-7. PubMed ID: 22219649
[TBL] [Abstract][Full Text] [Related]
8. A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma.
Parsam VL; Kannabiran C; Honavar S; Vemuganti GK; Ali MJ
J Genet; 2009 Dec; 88(4):517-27. PubMed ID: 20090211
[TBL] [Abstract][Full Text] [Related]
9. RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling.
Parma D; Ferrer M; Luce L; Giliberto F; Szijan I
PLoS One; 2017; 12(12):e0189736. PubMed ID: 29261756
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Genetic screening in Iranian patients with retinoblastoma.
Shahraki K; Ahani A; Sharma P; Faranoush M; Bahoush G; Torktaz I; Gahl WA; Naseripour M; Behnam B
Eye (Lond); 2017 Apr; 31(4):620-627. PubMed ID: 27983729
[TBL] [Abstract][Full Text] [Related]
12. [Low-penetrance retinoblastoma due to exons 24 and 25 deletions in the Rb1 gene].
Du C; Jiang Y; Gallie BL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Oct; 19(5):370-4. PubMed ID: 12362308
[TBL] [Abstract][Full Text] [Related]
13. Clinical characteristics and germline mutation spectrum of RB1 in Chinese patients with retinoblastoma: A dual-center study of 145 patients.
Chai P; Luo Y; Yu J; Li Y; Yang J; Zhuang A; Fan J; Han M; Jia R
Exp Eye Res; 2021 Apr; 205():108456. PubMed ID: 33493472
[TBL] [Abstract][Full Text] [Related]
14. Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastoma.
Mitter D; Rushlow D; Nowak I; Ansperger-Rescher B; Gallie BL; Lohmann DR
Fam Cancer; 2009; 8(1):55-8. PubMed ID: 18509746
[TBL] [Abstract][Full Text] [Related]
15. 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]
16.
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]
17. Novel mutations in the RB1 gene from Chinese families with a history of retinoblastoma.
Zhang L; Jia R; Zhao J; Fan J; Zhou Y; Han B; Song X; Wu L; Zhang H; Song H; Ge S; Fan X
Tumour Biol; 2015 Apr; 36(4):2409-20. PubMed ID: 25424699
[TBL] [Abstract][Full Text] [Related]
18. Attenuation of disease phenotype through alternative translation initiation in low-penetrance retinoblastoma.
Sánchez-Sánchez F; Ramírez-Castillejo C; Weekes DB; Beneyto M; Prieto F; Nájera C; Mittnacht S
Hum Mutat; 2007 Feb; 28(2):159-67. PubMed ID: 16988938
[TBL] [Abstract][Full Text] [Related]
19. Screening of RB1 gene mutations in Chinese patients with retinoblastoma and preliminary exploration of genotype-phenotype correlations.
He MY; An Y; Gao YJ; Qian XW; Li G; Qian J
Mol Vis; 2014; 20():545-52. PubMed ID: 24791139
[TBL] [Abstract][Full Text] [Related]
20. A possible hot spot in exon 21 of the retinoblastoma gene predisposing to a low penetrant retinoblastoma phenotype?
Ahmad NN; Melo MB; Singh AD; Donoso LA; Shields JA
Ophthalmic Genet; 1999 Dec; 20(4):225-31. PubMed ID: 10617920
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
