140 related articles for article (PubMed ID: 11277399)
1. A microsatellite fluorescent method for linkage analysis in familial retinoblastoma and deletion detection at the RB1 locus in retinoblastoma and osteosarcoma.
Alonso J; García-Miguel P; Abelairas J; Mendiola M; Pestaña A
Diagn Mol Pathol; 2001 Mar; 10(1):9-14. PubMed ID: 11277399
[TBL] [Abstract][Full Text] [Related]
2. Prediction of retinoblastoma and osteosarcoma: linkage analysis of families by using polymorphic markers around RB1 locus.
Chunder N; Basu D; Roy A; Roychoudhury S; Panda CK
J BUON; 2003; 8(4):365-9. PubMed ID: 17472278
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markers.
Girardet A; Hamamah S; Anahory T; Déchaud H; Sarda P; Hédon B; Demaille J; Claustres M
Mol Hum Reprod; 2003 Feb; 9(2):111-6. PubMed ID: 12569181
[TBL] [Abstract][Full Text] [Related]
6. Molecular studies of loss of heterozygosity in retinoblastoma.
Chiu LL; Lai PS; Low PS; Ling YL; Cheong PY; Chee CK; Wong PK; Lim AS
Ann Acad Med Singap; 1997 May; 26(3):315-9. PubMed ID: 9285025
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene.
Scheffer H; te Meerman GJ; Kruize YC; van den Berg AH; Penninga DP; Tan KE; der Kinderen DJ; Buys CH
Am J Hum Genet; 1989 Aug; 45(2):252-60. PubMed ID: 2569269
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. "Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma".
Quiñonez-Silva G; Dávalos-Salas M; Recillas-Targa F; Ostrosky-Wegman P; Aranda DA; Benítez-Bribiesca L
Clin Epigenetics; 2016; 8():1. PubMed ID: 26753011
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The survival gene MED4 explains low penetrance retinoblastoma in patients with large RB1 deletion.
Dehainault C; Garancher A; Castéra L; Cassoux N; Aerts I; Doz F; Desjardins L; Lumbroso L; Montes de Oca R; Almouzni G; Stoppa-Lyonnet D; Pouponnot C; Gauthier-Villars M; Houdayer C
Hum Mol Genet; 2014 Oct; 23(19):5243-50. PubMed ID: 24858910
[TBL] [Abstract][Full Text] [Related]
15. Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigrees.
Munier FL; Wang MX; Spence MA; Thonney F; Balmer A; Pescia G; Donoso LA; Murphree AL
Arch Ophthalmol; 1993 Nov; 111(11):1507-11. PubMed ID: 8240106
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Loss of heterozygosity and microsatellite instability at the retinoblastoma locus in osteosarcomas.
Belchis DA; Meece CA; Benko FA; Rogan PK; Williams RA; Gocke CD
Diagn Mol Pathol; 1996 Sep; 5(3):214-9. PubMed ID: 8866236
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Deletion of Rb1 gene in late osteosarcoma from survivor of unilateral retinoblastoma--a case report.
Lee SY; Jeon DG; Lee JS; Hwang CS; Huh K; Lee TW; Hong SI
J Korean Med Sci; 1996 Feb; 11(1):94-8. PubMed ID: 8703379
[TBL] [Abstract][Full Text] [Related]
20. Molecular genetic considerations in osteosarcoma.
Hansen MF
Clin Orthop Relat Res; 1991 Sep; (270):237-46. PubMed ID: 1679382
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]