These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
215 related articles for article (PubMed ID: 31997559)
1. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. [Clinical features of patients with retinocytoma]. Yi XQ; Qian J; Guo J; Xue K Zhonghua Yan Ke Za Zhi; 2021 Jul; 57(7):526-530. PubMed ID: 34256473 [No Abstract] [Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Ectopic intracranial retinoblastoma in a 3.5-month-old infant without eye involvement and without evidence of heritability. Römer T; Temming P; Lohmann DR; Sturm D; von Deimling A; Sellhaus B; Mull M; Kontny U; Moser O Pediatr Blood Cancer; 2019 May; 66(5):e27599. PubMed ID: 30604586 [TBL] [Abstract][Full Text] [Related]
20. Retinocytoma associated with calcified vitreous deposits. Hadjistilianou T; De Francesco S; Martone G; Malandrini A Eur J Ophthalmol; 2006; 16(2):349-51. PubMed ID: 16703560 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]