229 related articles for article (PubMed ID: 22103627)
1. Risk assessment of recurrence in sporadic retinoblastoma using a molecular-based algorithm.
Tran HV; Schorderet DF; Gaillard MC; Balmer A; Munier FL
Ophthalmic Genet; 2012 Mar; 33(1):6-11. PubMed ID: 22103627
[TBL] [Abstract][Full Text] [Related]
2. Linkage analysis and detection of somatic, postzygous RB1 mutations in Serbian retinoblastoma patients.
Kontic M; Palacios I; Kontic M; Alonso J; Pestana A
J BUON; 2011; 16(1):142-6. PubMed ID: 21674866
[TBL] [Abstract][Full Text] [Related]
3. Loss of heterozygosity and mutations are the major mechanisms of RB1 gene inactivation in Chinese with sporadic retinoblastoma.
Choy KW; Pang CP; Yu CB; Wong HL; Ng JS; Fan DS; Lo KW; Chai JT; Wang J; Fu W; Lam DS
Hum Mutat; 2002 Nov; 20(5):408. PubMed ID: 12402348
[TBL] [Abstract][Full Text] [Related]
4. [Molecular diagnosis of retinoblastoma. First experience in Russia].
Babenko OV; Brovkina AF; Zaletaev DV; Kozlova VM; Saakian SV; Nemtsova MV
Vestn Oftalmol; 2002; 118(1):28-31. PubMed ID: 11898356
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Low-penetrance retinoblastoma due to exons 24 and 25 deletions in the Rb1 gene].
Du C; Jiang Y; Gallie BL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Oct; 19(5):370-4. PubMed ID: 12362308
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Improved clinical management of retinoblastoma through gene testing.
Raizis A; Clemett R; Corbett R; McGaughran J; Evans J; George P
N Z Med J; 2002 May; 115(1154):231-4. PubMed ID: 12117173
[TBL] [Abstract][Full Text] [Related]
9. [Gene diagnosis and genetic counselling of Rb gene mutations in retinoblastoma patients and their family members].
Huang Q; Dryja TP; Yandell DW
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Apr; 15(2):65-8. PubMed ID: 9531640
[TBL] [Abstract][Full Text] [Related]
10. Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation.
Brichard B; Heusterspreute M; De Potter P; Chantrain C; Vermylen C; Sibille C; Gala JL
Eur J Cancer; 2006 Jan; 42(1):65-72. PubMed ID: 16343894
[TBL] [Abstract][Full Text] [Related]
11. Ten novel RB1 gene mutations in patients with retinoblastoma.
Abouzeid H; Munier FL; Thonney F; Schorderet DF
Mol Vis; 2007 Sep; 13():1740-5. PubMed ID: 17960112
[TBL] [Abstract][Full Text] [Related]
12. Molecular studies of loss of heterozygosity in Chinese sporadic retinoblastoma patients.
Zhang XL; Fu WL; Zhao HX; Zhou LX; Huang JF; Wang JH
Clin Chim Acta; 2005 Aug; 358(1-2):75-80. PubMed ID: 15921673
[TBL] [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. Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.
Nichols KE; Houseknecht MD; Godmilow L; Bunin G; Shields C; Meadows A; Ganguly A
Hum Mutat; 2005 Jun; 25(6):566-74. PubMed ID: 15884040
[TBL] [Abstract][Full Text] [Related]
15. Overview of RB gene mutations in patients with retinoblastoma. Implications for clinical genetic screening.
Harbour JW
Ophthalmology; 1998 Aug; 105(8):1442-7. PubMed ID: 9709755
[TBL] [Abstract][Full Text] [Related]
16. Genotype-phenotype correlations in hereditary familial retinoblastoma.
Taylor M; Dehainault C; Desjardins L; Doz F; Levy C; Sastre X; Couturier J; Stoppa-Lyonnet D; Houdayer C; Gauthier-Villars M
Hum Mutat; 2007 Mar; 28(3):284-93. PubMed ID: 17096365
[TBL] [Abstract][Full Text] [Related]
17. Screening for RB1 mutations in tumor tissue using denaturing high performance liquid chromatography, multiplex ligation-dependent probe amplification, and loss of heterozygosity analysis.
Sellner LN; Edkins E; Smith N
Pediatr Dev Pathol; 2006; 9(1):31-7. PubMed ID: 16808635
[TBL] [Abstract][Full Text] [Related]
18. Sporadic unilateral retinoblastoma or first sign of bilateral disease?
Temming P; Viehmann A; Biewald E; Lohmann DR
Br J Ophthalmol; 2013 Apr; 97(4):475-80. PubMed ID: 23355526
[TBL] [Abstract][Full Text] [Related]
19. RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling.
Parma D; Ferrer M; Luce L; Giliberto F; Szijan I
PLoS One; 2017; 12(12):e0189736. PubMed ID: 29261756
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
