BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

248 related articles for article (PubMed ID: 31715676)

  • 1. [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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Spectrum of germline
    Rojanaporn D; Boontawon T; Chareonsirisuthigul T; Thanapanpanich O; Attaseth T; Saengwimol D; Anurathapan U; Sujirakul T; Kaewkhaw R; Hongeng S
    Mol Vis; 2018; 24():778-788. PubMed ID: 30636860
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8.
    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
    [No Abstract]   [Full Text] [Related]  

  • 9. Mutational screening of germline
    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; 24():231-238. PubMed ID: 29568217
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. The
    Berry JL; Polski A; Cavenee WK; Dryja TP; Murphree AL; Gallie BL
    Genes (Basel); 2019 Nov; 10(11):. PubMed ID: 31683923
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.