174 related articles for article (PubMed ID: 29684226)
1. Iris Hypoplasia as the Presenting Sign of Retinoblastoma in a Child With a 13q Deletion.
Shah S; Koban Y; Le BHA; Bechtold M; Zolfaghari E; Kim JW; Berry JL
J Pediatr Ophthalmol Strabismus; 2018 Apr; 55():e10-e13. PubMed ID: 29684226
[TBL] [Abstract][Full Text] [Related]
2. Retinoblastoma in Patients with 13q deletion syndrome - case series.
Jedrychowska-Jamborska J; Morawski K; Kubicka-Trzaska A; Romanowska-Dixon B
Klin Oczna; 2016 Aug; 118(1):32-35. PubMed ID: 29715405
[TBL] [Abstract][Full Text] [Related]
3. Molecular diagnosis in patients with retinoblastoma: Report of a series of cases.
Ossandón D; Zanolli M; López JP; Benavides F; Pérez V; Repetto GM
Arch Soc Esp Oftalmol; 2016 Aug; 91(8):379-84. PubMed ID: 27021801
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Mud-splattered fundus.
Welch RJ; Li X; Shields CL
Indian J Ophthalmol; 2018 Apr; 66(4):573. PubMed ID: 29582825
[No Abstract] [Full Text] [Related]
6. A del(13)(q21.32q31.2)dn refined to 21.9 Mb in a female toddler with irides heterochromia and hypopigmentation: appraisal of interstitial mid-13q deletions.
Córdova-Fletes C; Rivera H; Garza-Villarreal EA; Vázquéz-Cárdenas NA; Martínez-Jacobo LA; Moreno-Andrade T
Clin Dysmorphol; 2017 Jan; 26(1):33-37. PubMed ID: 27750267
[No Abstract] [Full Text] [Related]
7. A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report.
Tsutsumi M; Hattori H; Akita N; Maeda N; Kubota T; Horibe K; Fujita N; Kawai M; Shinkai Y; Kato M; Kato T; Kawamura R; Suzuki F; Kurahashi H
BMC Med Genomics; 2019 Dec; 12(1):182. PubMed ID: 31806026
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Heterochromia following intravitreal chemotherapy in two cases.
Camp DA; Lally SE; Shields CL
J AAPOS; 2019 Aug; 23(4):241-243. PubMed ID: 31039403
[TBL] [Abstract][Full Text] [Related]
10. 13q deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twins.
De Francesco S; Galluzzi P; Del Longo A; Piozzi E; Renieri A; Menicacci C; Mari F; Munier F; Hadjistilianou T; Mastrangelo D
Eur J Ophthalmol; 2012; 22(5):857-60. PubMed ID: 22505049
[TBL] [Abstract][Full Text] [Related]
11. Bilateral asymmetrical partial heterochromia of iris and fundus in Waardenburg syndrome type 2A with a novel
Kumawat D; Kumar V; Sahay P; Nongrem G; Chandra P
Indian J Ophthalmol; 2019 Sep; 67(9):1481-1483. PubMed ID: 31436206
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Novel RB1 germline mutation in a healthy man.
Ramos-Dávila EM; Garza-Garza LA; Villafuerte-de la Cruz R; Aguilar-Y-Mendez D; Morales-Garza HJ; Garza-Leon M; Ruiz-Lozano RE; Ancona-Lezama D
Ophthalmic Genet; 2022 Aug; 43(4):561-566. PubMed ID: 35410579
[TBL] [Abstract][Full Text] [Related]
15. Heterochromia iridis with primary hypoparathyroidism.
Kumar R; Reddy DV; Unnikrishnan AG; Kapoor D; Agrawal NK; Singh SK
J Assoc Physicians India; 2004 Mar; 52():216. PubMed ID: 15636313
[No Abstract] [Full Text] [Related]
16. New onset of iris heterochromia and a limp.
Falzon K; Wood M; Long VW
J Pediatr; 2014 Jul; 165(1):200-200.e1. PubMed ID: 24704298
[No Abstract] [Full Text] [Related]
17. Iris Heterochromia.
Kirkwood BJ; Kirkwood RA
Insight; 2015; 40(3):12-6. PubMed ID: 26364498
[No Abstract] [Full Text] [Related]
18. Genetic testing in infantile spasms identifies a chromosome 13q deletion and retinoblastoma.
Jones K; Minassian BA
Pediatr Neurol; 2014 May; 50(5):522-4. PubMed ID: 24485929
[TBL] [Abstract][Full Text] [Related]
19. Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan.
Yousef YA; Tbakhi A; Al-Hussaini M; AlNawaiseh I; Saab A; Afifi A; Naji M; Mohammad M; Deebajah R; Jaradat I; Sultan I; Mehyar M
Fam Cancer; 2018 Apr; 17(2):261-268. PubMed ID: 28803391
[TBL] [Abstract][Full Text] [Related]
20. Loss of retinoblastoma in pleomorphic fibroma: An immunohistochemical and genomic analysis.
Hinds B; Agulló Pérez AD; LeBoit PE; McCalmont TH; North JP
J Cutan Pathol; 2017 Aug; 44(8):665-671. PubMed ID: 28543636
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]