229 related articles for article (PubMed ID: 34336010)
41. Targeted long-read sequencing allows for rapid identification of pathogenic disease-causing variants in retinoblastoma.
Nakamichi K; Stacey A; Mustafi D
Ophthalmic Genet; 2022 Dec; 43(6):762-770. PubMed ID: 36325802
[TBL] [Abstract][Full Text] [Related]
42. 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]
43. Variation of second cancer risk by family history of retinoblastoma among long-term survivors.
Kleinerman RA; Yu CL; Little MP; Li Y; Abramson D; Seddon J; Tucker MA
J Clin Oncol; 2012 Mar; 30(9):950-7. PubMed ID: 22355046
[TBL] [Abstract][Full Text] [Related]
44. 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]
45. 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]
46. 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]
47. Identification of 26 new constitutional RB1 gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients.
Alonso J; Frayle H; Menéndez I; López A; García-Miguel P; Abelairas J; Sarret E; Vendrell MT; Navajas A; Artigas M; Indiano JM; Carbone A; Torrenteras C; Palacios I; Pestaña A
Hum Mutat; 2005 Jan; 25(1):99. PubMed ID: 15605413
[TBL] [Abstract][Full Text] [Related]
48. Knudson's hypothesis revisited in Indian retinoblastoma patients.
Gaikwad N; Vanniarajan A; Husain A; Jeyaram I; Thirumalairaj K; Santhi R; Muthukkaruppan V; Kim U
Asia Pac J Clin Oncol; 2015 Dec; 11(4):299-307. PubMed ID: 26264229
[TBL] [Abstract][Full Text] [Related]
49. Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma.
Amare Kadam PS; Ghule P; Jose J; Bamne M; Kurkure P; Banavali S; Sarin R; Advani S
Cancer Genet Cytogenet; 2004 Apr; 150(1):33-43. PubMed ID: 15041221
[TBL] [Abstract][Full Text] [Related]
50. Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastoma.
Mitter D; Rushlow D; Nowak I; Ansperger-Rescher B; Gallie BL; Lohmann DR
Fam Cancer; 2009; 8(1):55-8. PubMed ID: 18509746
[TBL] [Abstract][Full Text] [Related]
51. Constitutional retinoblastoma gene deletion in Egyptian patients.
Mohammed AM; Kamel AK; Hammad SA; Afifi HH; El Sanabary Z; El Din ME
World J Pediatr; 2009 Aug; 5(3):222-5. PubMed ID: 19693468
[TBL] [Abstract][Full Text] [Related]
52. Deletion of Rb1 gene in late osteosarcoma from survivor of unilateral retinoblastoma--a case report.
Lee SY; Jeon DG; Lee JS; Hwang CS; Huh K; Lee TW; Hong SI
J Korean Med Sci; 1996 Feb; 11(1):94-8. PubMed ID: 8703379
[TBL] [Abstract][Full Text] [Related]
53. Unilateral retinocytoma associated with a variant in the RB1 gene.
Wu S; Zou X; Sun Z; Zhu T; Wei X; Sui R
Mol Genet Genomic Med; 2020 Apr; 8(4):e1156. PubMed ID: 31997559
[TBL] [Abstract][Full Text] [Related]
54. Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma.
Grotta S; D'Elia G; Scavelli R; Genovese S; Surace C; Sirleto P; Cozza R; Romanzo A; De Ioris MA; Valente P; Tomaiuolo AC; Lepri FR; Franchin T; Ciocca L; Russo S; Locatelli F; Angioni A
BMC Cancer; 2015 Nov; 15():841. PubMed ID: 26530098
[TBL] [Abstract][Full Text] [Related]
55. 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]
56. Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastoma.
Munier FL; Thonney F; Balmer A; Uffer S; Héon E; Van Melle G; Rutz HP; Pescia G; Schorderet DF
Ophthalmic Genet; 1997 Mar; 18(1):7-12. PubMed ID: 9134545
[TBL] [Abstract][Full Text] [Related]
57. The genetics of retinoblastoma. Relevance to the patient.
Gallie BL; Dunn JM; Chan HS; Hamel PA; Phillips RA
Pediatr Clin North Am; 1991 Apr; 38(2):299-315. PubMed ID: 2006079
[TBL] [Abstract][Full Text] [Related]
58. Spectrum of RB1 mutations in argentine patients: 20-years experience in the molecular diagnosis of retinoblastoma.
Ottaviani D; Parma D; Giliberto F; Ferrer M; Fandino A; Davila MT; Chantada G; Szijan I
Ophthalmic Genet; 2013 Dec; 34(4):189-98. PubMed ID: 23301675
[TBL] [Abstract][Full Text] [Related]
59. Spectrum of RB1 mutations identified in 403 retinoblastoma patients.
Price EA; Price K; Kolkiewicz K; Hack S; Reddy MA; Hungerford JL; Kingston JE; Onadim Z
J Med Genet; 2014 Mar; 51(3):208-14. PubMed ID: 24225018
[TBL] [Abstract][Full Text] [Related]
60. Molecular biology of retinoblastoma.
Sábado Alvarez C
Clin Transl Oncol; 2008 Jul; 10(7):389-94. PubMed ID: 18628066
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
