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Journal Abstract Search

235 related items for PubMed ID: 34645364

  • 1. Identification of novel RB1 genetic variants in Retinoblastoma patients and their impact on clinical outcome.
    Manukonda R, Pujar A, Ramappa G, Vemuganti GK, Kaliki S.
    Ophthalmic Genet; 2022 Feb; 43(1):64-72. PubMed ID: 34645364
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  • 2. Spectrum of germline RB1 mutations and clinical manifestations in retinoblastoma patients from Thailand.
    Rojanaporn D, Boontawon T, Chareonsirisuthigul T, Thanapanpanich O, Attaseth T, Saengwimol D, Anurathapan U, Sujirakul T, Kaewkhaw R, Hongeng S.
    Mol Vis; 2018 Feb; 24():778-788. PubMed ID: 30636860
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  • 3. 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 Feb; 27():1-16. PubMed ID: 33456302
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  • 5. Mutational screening of germline RB1 gene in Vietnamese patients with retinoblastoma reveals three novel mutations.
    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 Feb; 24():231-238. PubMed ID: 29568217
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  • 9. RB1 germline mutation spectrum and clinical features in patients with unilateral retinoblastomas.
    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
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  • 11. 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 Oct; 22():1036-47. PubMed ID: 27582626
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  • 12. Simultaneous identification of clinically relevant RB1 mutations and copy number alterations in aqueous humor of retinoblastoma eyes.
    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
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  • 13. 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
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  • 17. Multiplex ligation-dependent probe amplification versus fluorescent in situ hybridization for screening RB1 copy number variations in Egyptian patients with retinoblastoma.
    Eid OM, El Zomor H, Mohamed AM, El-Bassyouni HT, Afifi HH, El-Ayadi M, Sadek SH, Hammad SA, Salem SI, Mahrous R, Fadel IM, Refaat K, Afifi MA, Shelil AE, Ziko OAO, Abdel Azeem AA, El-Haddad A.
    Ophthalmic Genet; 2022 Dec; 43(6):789-794. PubMed ID: 36098066
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  • 19. Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis.
    Kalsoom S, Wasim M, Afzal S, Shahzad MS, Ramzan S, Awan AR, Anjum AA, Ramzan K.
    Mol Vis; 2015 Dec; 21():1085-92. PubMed ID: 26396485
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  • 20. 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
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