215 related articles for article (PubMed ID: 29470311)
1. ROUTINE FUNDUS SCREENING OF FAMILIES OF CHILDREN WITH RETINOBLASTOMA: A Prospective Study of 131 Consecutive Families.
Kaliki S; Gupta Rathi S; Patel A
Retina; 2019 Jul; 39(7):1326-1332. PubMed ID: 29470311
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan.
Yousef YA; Tbakhi A; Al-Hussaini M; AlNawaiseh I; Saab A; Afifi A; Naji M; Mohammad M; Deebajah R; Jaradat I; Sultan I; Mehyar M
Fam Cancer; 2018 Apr; 17(2):261-268. PubMed ID: 28803391
[TBL] [Abstract][Full Text] [Related]
6. Impact of RB1 gene screening from blood collected on a single day from 411 family members of 113 Retinoblastoma survivors in India.
Vanniarajan A; Maitra P; Saraswathi KK; Shah PK
Eye (Lond); 2024 Jun; 38(8):1575-1580. PubMed ID: 38341497
[TBL] [Abstract][Full Text] [Related]
7. Association Between Genotype and Phenotype in Consecutive Unrelated Individuals With Retinoblastoma.
Salviat F; Gauthier-Villars M; Carton M; Cassoux N; Lumbroso-Le Rouic L; Dehainault C; Levy C; Golmard L; Aerts I; Doz F; Bonnet-Serrano F; Hayek S; Savignoni A; Stoppa-Lyonnet D; Houdayer C
JAMA Ophthalmol; 2020 Aug; 138(8):843-850. PubMed ID: 32556071
[TBL] [Abstract][Full Text] [Related]
8. Lack of correlation between age at diagnosis and RB1 mutations for unilateral retinoblastoma: the importance of genetic testing.
Berry JL; Lewis L; Zolfaghari E; Green S; Le BHA; Lee TC; Murphree AL; Kim JW; Jubran R
Ophthalmic Genet; 2018 Jun; 39(3):407-409. PubMed ID: 29286867
[No Abstract] [Full Text] [Related]
9. Novel RB1 germline mutation in a healthy man.
Ramos-Dávila EM; Garza-Garza LA; Villafuerte-de la Cruz R; Aguilar-Y-Mendez D; Morales-Garza HJ; Garza-Leon M; Ruiz-Lozano RE; Ancona-Lezama D
Ophthalmic Genet; 2022 Aug; 43(4):561-566. PubMed ID: 35410579
[TBL] [Abstract][Full Text] [Related]
10.
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]
11. RB1 screening of retinoblastoma patients in Sri Lanka using targeted next generation sequencing (NGS) and gene ratio analysis copy enumeration PCR (GRACE-PCR).
Kugalingam N; De Silva D; Abeysekera H; Nanayakkara S; Tirimanne S; Ranaweera D; Suravajhala P; Chandrasekharan V
BMC Med Genomics; 2023 Nov; 16(1):279. PubMed ID: 37932687
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Variability in retinoblastoma genome stability is driven by age and not heritability.
Polski A; Xu L; Prabakar RK; Gai X; Kim JW; Shah R; Jubran R; Kuhn P; Cobrinik D; Hicks J; Berry JL
Genes Chromosomes Cancer; 2020 Oct; 59(10):584-590. PubMed ID: 32390242
[TBL] [Abstract][Full Text] [Related]
14. Germline RB1 Mutation in Retinoblastoma Patients: Detection Methods and Implication in Tumor Focality.
Rojanaporn D; Chitphuk S; Iemwimangsa N; Chareonsirisuthigul T; Saengwimol D; Aroonroch R; Anurathathapan U; Hongeng S; Kaewkhaw R
Transl Vis Sci Technol; 2022 Sep; 11(9):30. PubMed ID: 36173648
[TBL] [Abstract][Full Text] [Related]
15. Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.
Singh J; Mishra A; Pandian AJ; Mallipatna AC; Khetan V; Sripriya S; Kapoor S; Agarwal S; Sankaran S; Katragadda S; Veeramachaneni V; Hariharan R; Subramanian K; Mannan AU
Mol Vis; 2016; 22():1036-47. PubMed ID: 27582626
[TBL] [Abstract][Full Text] [Related]
16. Identification of novel RB1 genetic variants in Retinoblastoma patients and their impact on clinical outcome.
Manukonda R; Pujar A; Ramappa G; Vemuganti GK; Kaliki S
Ophthalmic Genet; 2022 Feb; 43(1):64-72. PubMed ID: 34645364
[TBL] [Abstract][Full Text] [Related]
17. Risk assessment of recurrence in sporadic retinoblastoma using a molecular-based algorithm.
Tran HV; Schorderet DF; Gaillard MC; Balmer A; Munier FL
Ophthalmic Genet; 2012 Mar; 33(1):6-11. PubMed ID: 22103627
[TBL] [Abstract][Full Text] [Related]
18. Patient understanding of genetic information influences reproductive decision making in retinoblastoma.
Foster A; Boyes L; Burgess L; Carless S; Bowyer V; Jenkinson H; Parulekar M; Ainsworth J; Hungerford J; Onadim Z; Sagoo M; Rosser E; Reddy MA; Cole T
Clin Genet; 2017 Dec; 92(6):587-593. PubMed ID: 28397259
[TBL] [Abstract][Full Text] [Related]
19. Prognostic Information for Known Genetic Carriers of RB1 Pathogenic Variants (Germline and Mosaic).
Reddy MA; Butt M; Hinds AM; Duncan C; Price EA; Sagoo MS; Onadim Z
Ophthalmol Retina; 2021 Apr; 5(4):381-387. PubMed ID: 32835838
[TBL] [Abstract][Full Text] [Related]
20. Detection and reporting of RB1 promoter hypermethylation in diagnostic screening.
Price EA; Kolkiewicz K; Patel R; Hashim S; Karaa E; Scheimberg I; Sagoo MS; Reddy MA; Onadim Z
Ophthalmic Genet; 2018 Aug; 39(4):526-531. PubMed ID: 29851531
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
