165 related articles for article (PubMed ID: 12419581)
1. Identification of novel mutations in the RB1 gene in Mexican patients with retinoblastoma.
Rodríguez M; Salcedo M; González M; Coral-Vazquez R; Salamanca F; Arenas D
Cancer Genet Cytogenet; 2002 Oct; 138(1):27-31. PubMed ID: 12419581
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis.
Kalsoom S; Wasim M; Afzal S; Shahzad MS; Ramzan S; Awan AR; Anjum AA; Ramzan K
Mol Vis; 2015; 21():1085-92. PubMed ID: 26396485
[TBL] [Abstract][Full Text] [Related]
8. [Genomic retinoblastoma perspectives: implications of tumor supressor gene RB1].
Rodríguez-Cruz M; del Prado M; Salcedo M
Rev Invest Clin; 2005; 57(4):572-81. PubMed ID: 16315642
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Germline mutations in the RB1 gene in patients with hereditary retinoblastoma.
Liu Z; Song Y; Bia B; Cowell JK
Genes Chromosomes Cancer; 1995 Dec; 14(4):277-84. PubMed ID: 8605116
[TBL] [Abstract][Full Text] [Related]
11. Detection of mutations in the RB1 gene by single strand conformation polymorphism (SSCP) analysis, amplification mismatch detection (AMD) analysis and polymerase chain reaction sequencing.
Dundar M; Lanyon GW; Connor MJ
Proc Natl Sci Counc Repub China B; 2001 Jul; 25(3):166-73. PubMed ID: 11480772
[TBL] [Abstract][Full Text] [Related]
12. Identification of 26 new constitutional RB1 gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients.
Alonso J; Frayle H; Menéndez I; López A; García-Miguel P; Abelairas J; Sarret E; Vendrell MT; Navajas A; Artigas M; Indiano JM; Carbone A; Torrenteras C; Palacios I; Pestaña A
Hum Mutat; 2005 Jan; 25(1):99. PubMed ID: 15605413
[TBL] [Abstract][Full Text] [Related]
13. Novel RB1 gene constitutional mutations found in Polish patients with familial and/or bilateral retinoblastoma.
Jakubowska A; Zajaczek S; Haus O; Limon J; Kostyk E; Krzystolik Z; Lubinski J
Hum Mutat; 2001 Nov; 18(5):459. PubMed ID: 11668642
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Enhanced sensitivity for detection of low-level germline mosaic RB1 mutations in sporadic retinoblastoma cases using deep semiconductor sequencing.
Chen Z; Moran K; Richards-Yutz J; Toorens E; Gerhart D; Ganguly T; Shields CL; Ganguly A
Hum Mutat; 2014 Mar; 35(3):384-91. PubMed ID: 24282159
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma.
Parsam VL; Kannabiran C; Honavar S; Vemuganti GK; Ali MJ
J Genet; 2009 Dec; 88(4):517-27. PubMed ID: 20090211
[TBL] [Abstract][Full Text] [Related]
19. Identification of three novel RB1 mutations in Brazilian patients with retinoblastoma by "exon by exon" PCR mediated SSCP analysis.
Braggio E; Bonvicino CR; Vargas FR; Ferman S; Eisenberg AL; Seuánez HN
J Clin Pathol; 2004 Jun; 57(6):585-90. PubMed ID: 15166261
[TBL] [Abstract][Full Text] [Related]
20. Mutational screening of the RB1 gene in Italian patients with retinoblastoma reveals 11 novel mutations.
Sampieri K; Hadjistilianou T; Mari F; Speciale C; Mencarelli MA; Cetta F; Manoukian S; Peissel B; Giachino D; Pasini B; Acquaviva A; Caporossi A; Frezzotti R; Renieri A; Bruttini M
J Hum Genet; 2006; 51(3):209-216. PubMed ID: 16463005
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]