156 related articles for article (PubMed ID: 32273112)
1. Same Mutation, Earlier Detection.
Yaghy A; Eiger-Moscovich M; Shields CL
Ophthalmol Retina; 2020 Apr; 4(4):402. PubMed ID: 32273112
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Aqueous Humor Is Superior to Blood as a Liquid Biopsy for Retinoblastoma.
Berry JL; Xu L; Polski A; Jubran R; Kuhn P; Kim JW; Hicks J
Ophthalmology; 2020 Apr; 127(4):552-554. PubMed ID: 31767439
[TBL] [Abstract][Full Text] [Related]
6. Mud-splattered fundus.
Welch RJ; Li X; Shields CL
Indian J Ophthalmol; 2018 Apr; 66(4):573. PubMed ID: 29582825
[No Abstract] [Full Text] [Related]
7. [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]
8. 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]
9. 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]
10. Genetics of Retinoblastoma.
Mallipatna A; Marino M; Singh AD
Asia Pac J Ophthalmol (Phila); 2016; 5(4):260-4. PubMed ID: 27488068
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Iris Hypoplasia as the Presenting Sign of Retinoblastoma in a Child With a 13q Deletion.
Shah S; Koban Y; Le BHA; Bechtold M; Zolfaghari E; Kim JW; Berry JL
J Pediatr Ophthalmol Strabismus; 2018 Apr; 55():e10-e13. PubMed ID: 29684226
[TBL] [Abstract][Full Text] [Related]
13. Retinoblastoma genetics in India: From research to implementation.
Dimaras H
Indian J Ophthalmol; 2015 Mar; 63(3):219-26. PubMed ID: 25971166
[TBL] [Abstract][Full Text] [Related]
14. Mature Ovarian Teratoma After Treatment for Unilateral Retinoblastoma With Nonmutated RB1.
Collins B; Corey SJ
J Pediatr Hematol Oncol; 2017 Aug; 39(6):485-486. PubMed ID: 28719514
[No Abstract] [Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. Ectopic intracranial retinoblastoma in a 3.5-month-old infant without eye involvement and without evidence of heritability.
Römer T; Temming P; Lohmann DR; Sturm D; von Deimling A; Sellhaus B; Mull M; Kontny U; Moser O
Pediatr Blood Cancer; 2019 May; 66(5):e27599. PubMed ID: 30604586
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]