338 related articles for article (PubMed ID: 28397259)
1. 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]
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. Prenatal genetic diagnosis of retinoblastoma and report of RB1 gene mutation from India.
Shah PK; Sripriya S; Narendran V; Pandian AJ
Ophthalmic Genet; 2016 Dec; 37(4):430-433. PubMed ID: 26914665
[TBL] [Abstract][Full Text] [Related]
5. Danish retinoblastoma patients 1943-2013 - genetic testing and clinical implications.
Gregersen PA; Urbak SF; Funding M; Overgaard J; Jensen UB; Alsner J
Acta Oncol; 2016; 55(4):412-7. PubMed ID: 26494512
[TBL] [Abstract][Full Text] [Related]
6.
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]
7. 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]
8. [Promoting regulated gene diagnosis for retinoblastoma in clinical work].
Liang JH; Zhu XM
Zhonghua Yan Ke Za Zhi; 2019 Nov; 55(11):806-810. PubMed ID: 31715676
[TBL] [Abstract][Full Text] [Related]
9. Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features.
Afshar AR; Pekmezci M; Bloomer MM; Cadenas NJ; Stevers M; Banerjee A; Roy R; Olshen AB; Van Ziffle J; Onodera C; Devine WP; Grenert JP; Bastian BC; Solomon DA; Damato BE
Ophthalmology; 2020 Jun; 127(6):804-813. PubMed ID: 32139107
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A novel deep intronic low penetrance RB1 variant in a retinoblastoma family.
Soliman SE; Racher H; Lambourne M; Matevski D; MacDonald H; Gallie B
Ophthalmic Genet; 2018 Apr; 39(2):288-290. PubMed ID: 29099630
[No Abstract] [Full Text] [Related]
12. 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]
13. Knowledge of genetics in familial retinoblastoma.
Soliman SE; ElManhaly M; Dimaras H
Ophthalmic Genet; 2017; 38(3):226-232. PubMed ID: 27427836
[TBL] [Abstract][Full Text] [Related]
14. Next generation sequencing of RB1gene for the molecular diagnosis of ethnic minority with retinoblastoma in Yunnan.
Zhang Z; Xiao YS; Shen R; Jiang HC; Tan L; Li RQ; Yang XH; Gu HY; He WJ; Ma J
BMC Med Genet; 2020 Nov; 21(1):230. PubMed ID: 33225895
[TBL] [Abstract][Full Text] [Related]
15. Bilateral retinoblastoma due to a germline mutation of RB1 in a child with down syndrome.
Le Grignou M; Bleriot A; Nizon M; Pacquement H; Houdayer C; Thebaud E; Le Meur G; Isidor B
Ophthalmic Genet; 2019 Feb; 40(1):86. PubMed ID: 30822236
[No Abstract] [Full Text] [Related]
16. A novel de-novo RB1 mutation identified in a patient with bilateral retinoblastoma.
Fukushima H; Suzuki R; Hiraoka T; Suzuki S; Noguchi E; Takada H
Jpn J Clin Oncol; 2023 Aug; 53(9):863-865. PubMed ID: 37345682
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
