206 related articles for article (PubMed ID: 32835838)
21. 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]
22. 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]
23. 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]
24. Optical Coherence Tomography-Guided Decisions in Retinoblastoma Management.
Soliman SE; VandenHoven C; MacKeen LD; Héon E; Gallie BL
Ophthalmology; 2017 Jun; 124(6):859-872. PubMed ID: 28318638
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Impact of RB1 gene mutation type in retinoblastoma patients on clinical presentation and management outcome.
Mehyar M; Mosallam M; Tbakhi A; Saab A; Sultan I; Deebajah R; Jaradat I; AlJabari R; Mohammad M; AlNawaiseh I; Al-Hussaini M; Yousef YA
Hematol Oncol Stem Cell Ther; 2020 Sep; 13(3):152-159. PubMed ID: 32222358
[TBL] [Abstract][Full Text] [Related]
27. The impact of RB1 genotype on incidence of second tumours in heritable retinoblastoma.
Ketteler P; Hülsenbeck I; Frank M; Schmidt B; Jöckel KH; Lohmann DR
Eur J Cancer; 2020 Jul; 133():47-55. PubMed ID: 32434110
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. 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]
31. Simultaneous identification of clinically relevant
Xu L; Shen L; Polski A; Prabakar RK; Shah R; Jubran R; Kim JW; Biegel J; Kuhn P; Cobrinik D; Hicks J; Gai X; Berry JL
Ophthalmic Genet; 2020 Dec; 41(6):526-532. PubMed ID: 32799607
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. Molecular alterations in retinoblastoma beyond RB1.
Mendonça V; Evangelista AC; P Matta B; M Moreira MÂ; Faria P; Lucena E; Seuánez HN
Exp Eye Res; 2021 Oct; 211():108753. PubMed ID: 34478740
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. "Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma".
Quiñonez-Silva G; Dávalos-Salas M; Recillas-Targa F; Ostrosky-Wegman P; Aranda DA; Benítez-Bribiesca L
Clin Epigenetics; 2016; 8():1. PubMed ID: 26753011
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. 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]
40. Osteosarcoma without prior retinoblastoma related to RB1 low-penetrance germline pathogenic variants: A novel type of RB1-related hereditary predisposition syndrome?
Imbert-Bouteille M; Gauthier-Villars M; Leroux D; Meunier I; Aerts I; Lumbroso-Le Rouic L; Lejeune S; Delnatte C; Abadie C; Pujol P; Houdayer C; Corsini C
Mol Genet Genomic Med; 2019 Dec; 7(12):e913. PubMed ID: 31568710
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]