301 related articles for article (PubMed ID: 27021801)
21. Molecular diagnosis of retinoblastoma by circulating tumor DNA analysis.
Jiménez I; Frouin É; Chicard M; Dehainault C; Le Gall J; Benoist C; Gauthier A; Lapouble E; Houdayer C; Radvanyi F; Bernard V; Brisse HJ; Gauthier-Villars M; Stoppa-Lyonnet D; Baulande S; Cassoux N; Lumbroso L; Matet A; Aerts I; Renault V; Doz F; Golmard L; Delattre O; Schleiermacher G
Eur J Cancer; 2021 Sep; 154():277-287. PubMed ID: 34298378
[TBL] [Abstract][Full Text] [Related]
22. [Genomic retinoblastoma perspectives: implications of tumor supressor gene RB1].
Rodríguez-Cruz M; del Prado M; Salcedo M
Rev Invest Clin; 2005; 57(4):572-81. PubMed ID: 16315642
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. 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]
26. 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]
27. 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]
28. Genetic testing in Tunisian families with heritable retinoblastoma using a low cost approach permits accurate risk prediction in relatives and reveals incomplete penetrance in adults.
Ayari Jeridi H; Bouguila H; Ansperger-Rescher B; Baroudi O; Mdimegh I; Omran I; Charradi K; Bouzayene H; Benammar-Elgaaïed A; Lohmann DR
Exp Eye Res; 2014 Jul; 124():48-55. PubMed ID: 24810223
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. [Genetics of retinoblastoma].
Minoda K
Nihon Rinsho; 1995 Nov; 53(11):2774-8. PubMed ID: 8538043
[TBL] [Abstract][Full Text] [Related]
31. Constitutional and somatic RB1 mutation spectrum in nonfamilial unilateral and bilateral retinoblastoma in India.
Bamne MN; Ghule PN; Jose J; Banavali SD; Kurkure PA; Amare Kadam PS
Genet Test; 2005; 9(3):200-11. PubMed ID: 16225399
[TBL] [Abstract][Full Text] [Related]
32. Frequency of 13q abnormalities among 203 patients with retinoblastoma.
Bunin GR; Emanuel BS; Meadows AT; Buckley JD; Woods WG; Hammond GD
J Natl Cancer Inst; 1989 Mar; 81(5):370-4. PubMed ID: 2915374
[TBL] [Abstract][Full Text] [Related]
33. A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families.
Li WL; Buckley J; Sanchez-Lara PA; Maglinte DT; Viduetsky L; Tatarinova TV; Aparicio JG; Kim JW; Au M; Ostrow D; Lee TC; O'Gorman M; Judkins A; Cobrinik D; Triche TJ
J Mol Diagn; 2016 Jul; 18(4):480-93. PubMed ID: 27155049
[TBL] [Abstract][Full Text] [Related]
34. Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma.
Imperatore V; Pinto AM; Gelli E; Trevisson E; Morbidoni V; Frullanti E; Hadjistilianou T; De Francesco S; Toti P; Gusson E; Roversi G; Accogli A; Capra V; Mencarelli MA; Renieri A; Ariani F
Eur J Hum Genet; 2018 Jul; 26(7):1026-1037. PubMed ID: 29662154
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. Genetics and cytogenetics of retinoblastoma.
Cowell JK; Hogg A
Cancer Genet Cytogenet; 1992 Nov; 64(1):1-11. PubMed ID: 1458443
[No Abstract] [Full Text] [Related]
38. Bilateral retinoblastoma associated with 13q-mosaicism. Possible manifestation of a germinal mutation.
Ribeiro MC; Andrade JA; Erwenne CM; Brunoni D
Cancer Genet Cytogenet; 1988 Jun; 32(2):169-75. PubMed ID: 3365680
[TBL] [Abstract][Full Text] [Related]
39. Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.
Ramprasad VL; Madhavan J; Murugan S; Sujatha J; Suresh S; Sharma T; Kumaramanickavel G
Mol Diagn Ther; 2007; 11(1):63-70. PubMed ID: 17286451
[TBL] [Abstract][Full Text] [Related]
40. Preferential germline mutation of the paternal allele in retinoblastoma.
Zhu XP; Dunn JM; Phillips RA; Goddard AD; Paton KE; Becker A; Gallie BL
Nature; 1989 Jul; 340(6231):312-3. PubMed ID: 2568588
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
