320 related articles for article (PubMed ID: 9311732)
1. Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.
Lohmann DR; Gerick M; Brandt B; Oelschläger U; Lorenz B; Passarge E; Horsthemke B
Am J Hum Genet; 1997 Aug; 61(2):282-94. PubMed ID: 9311732
[TBL] [Abstract][Full Text] [Related]
2. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
Serrano ML; Yunis JJ
Biomedica; 2013; 33(1):53-61. PubMed ID: 23715307
[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. Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastoma.
Munier FL; Thonney F; Balmer A; Uffer S; Héon E; Van Melle G; Rutz HP; Pescia G; Schorderet DF
Ophthalmic Genet; 1997 Mar; 18(1):7-12. PubMed ID: 9134545
[TBL] [Abstract][Full Text] [Related]
5. Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma.
Greger V; Debus N; Lohmann D; Höpping W; Passarge E; Horsthemke B
Hum Genet; 1994 Nov; 94(5):491-6. PubMed ID: 7959682
[TBL] [Abstract][Full Text] [Related]
6. RB1 germ-line deletions in Argentine retinoblastoma patients.
Fernández C; Repetto K; Dalamon V; Bergonzi F; Ferreiro V; Szijan I
Mol Diagn Ther; 2007; 11(1):55-61. PubMed ID: 17286450
[TBL] [Abstract][Full Text] [Related]
7. Detection of mutations of the RB1 gene in retinoblastoma patients by using exon-by-exon PCR-SSCP analysis.
Shimizu T; Toguchida J; Kato MV; Kaneko A; Ishizaki K; Sasaki MS
Am J Hum Genet; 1994 May; 54(5):793-800. PubMed ID: 8178820
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. [Molecular genetics and diagnosis of retinoblastoma. Significance for ophthalmologic practice].
Lohmann DR; Brandt B; Passarge E; Horsthemke B
Ophthalmologe; 1997 Apr; 94(4):263-7. PubMed ID: 9229493
[TBL] [Abstract][Full Text] [Related]
11. Constitutional nonsense germline mutations in the RB1 gene detected in patients with early onset unilateral retinoblastoma.
Cowell JK; Cragg H
Eur J Cancer; 1996 Sep; 32A(10):1749-52. PubMed ID: 8983285
[TBL] [Abstract][Full Text] [Related]
12. A molecular study of first and second RB1 mutational hits in retinoblastoma patients.
de Andrade AF; da Hora Barbosa R; Vargas FR; Ferman S; Eisenberg AL; Fernandes L; Bonvicino CR
Cancer Genet Cytogenet; 2006 May; 167(1):43-6. PubMed ID: 16682285
[TBL] [Abstract][Full Text] [Related]
13. Constitutional and somatic RB1 mutation spectrum in nonfamilial unilateral and bilateral retinoblastoma in India.
Bamne MN; Ghule PN; Jose J; Banavali SD; Kurkure PA; Amare Kadam PS
Genet Test; 2005; 9(3):200-11. PubMed ID: 16225399
[TBL] [Abstract][Full Text] [Related]
14. Preliminary report of molecular detection of retinoblastoma gene mutations.
Zeng R; Jiang X; Zhang Q; Hu B; Chen Y
Yan Ke Xue Bao; 1994 Mar; 10(1):1-5. PubMed ID: 7843377
[TBL] [Abstract][Full Text] [Related]
15. [Genetics of retinoblastoma].
Minoda K
Nihon Rinsho; 1995 Nov; 53(11):2774-8. PubMed ID: 8538043
[TBL] [Abstract][Full Text] [Related]
16. Spectrum of RB1 gene mutations and loss of heterozygosity in Mexican patients with retinoblastoma: identification of six novel mutations.
Macías M; Dean M; Atkinson A; Jiménez-Morales S; García-Vazquez FJ; Saldaña-Alvarez Y; Ramírez-Bello J; Chávez M; Orozco L
Cancer Biomark; 2008; 4(2):93-9. PubMed ID: 18503160
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.
Ramprasad VL; Madhavan J; Murugan S; Sujatha J; Suresh S; Sharma T; Kumaramanickavel G
Mol Diagn Ther; 2007; 11(1):63-70. PubMed ID: 17286451
[TBL] [Abstract][Full Text] [Related]
20. Mechanisms of loss of heterozygosity in retinoblastoma.
Zhu X; Dunn JM; Goddard AD; Squire JA; Becker A; Phillips RA; Gallie BL
Cytogenet Cell Genet; 1992; 59(4):248-52. PubMed ID: 1544317
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]