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225 related items for PubMed ID: 17286451

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. [Prediction of retinoblastoma: linkage analysis of families with hereditary retinoblastoma by using polymorphic sites within the Rb gene].
    Yuan L, Gao Y, Lo S, Fang B, Ye J.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Oct; 17(5):338-42. PubMed ID: 8706167
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
    Serrano ML, Yunis JJ.
    Biomedica; 2013 Aug; 33(1):53-61. PubMed ID: 23715307
    [Abstract] [Full Text] [Related]

  • 6. Spectrum of germline RB1 mutations and clinical manifestations in retinoblastoma patients from Thailand.
    Rojanaporn D, Boontawon T, Chareonsirisuthigul T, Thanapanpanich O, Attaseth T, Saengwimol D, Anurathapan U, Sujirakul T, Kaewkhaw R, Hongeng S.
    Mol Vis; 2018 Aug; 24():778-788. PubMed ID: 30636860
    [Abstract] [Full Text] [Related]

  • 7. Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresis.
    Lohmann D, Horsthemke B, Gillessen-Kaesbach G, Stefani FH, Höfler H.
    Hum Genet; 1992 Apr; 89(1):49-53. PubMed ID: 1577465
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. 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 May; 9(1):31-7. PubMed ID: 16808635
    [Abstract] [Full Text] [Related]

  • 12. [Clinical applications of molecular diagnosis of retinoblastoma ain 15 families].
    Lendi B, Pescia G, Thonney F, Balmer A, Munier F.
    Klin Monbl Augenheilkd; 1995 May; 206(5):336-8. PubMed ID: 7609380
    [Abstract] [Full Text] [Related]

  • 13. PCR detection of Xbal polymorphism in the human Rb gene of retinoblastoma patients.
    Costanzi E, Erwenne CM, Armelin MC.
    Braz J Med Biol Res; 1993 Oct; 26(10):1031-6. PubMed ID: 7906172
    [Abstract] [Full Text] [Related]

  • 14. The polymerase chain reaction (PCR) in the routine genetic characterization of retinoblastoma: a tool for the clinical laboratory.
    Mastrangelo D, Squitieri N, Bruni S, Hadjistilianou T, Frezzotti R.
    Surv Ophthalmol; 1997 Oct; 41(4):331-40. PubMed ID: 9104770
    [Abstract] [Full Text] [Related]

  • 15. RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling.
    Parma D, Ferrer M, Luce L, Giliberto F, Szijan I.
    PLoS One; 2017 Oct; 12(12):e0189736. PubMed ID: 29261756
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. Human pituitary adenomas show no loss of heterozygosity at the retinoblastoma gene locus.
    Zhu J, Leon SP, Beggs AH, Busque L, Gilliland DG, Black PM.
    J Clin Endocrinol Metab; 1994 Apr; 78(4):922-7. PubMed ID: 8157722
    [Abstract] [Full Text] [Related]

  • 18. Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counseling.
    Munier FL, Thonney F, Balmer A, Héon E, Pescia G, Schorderet DF.
    Klin Monbl Augenheilkd; 1996 May; 208(5):400-3. PubMed ID: 8766064
    [Abstract] [Full Text] [Related]

  • 19. RB1 germ-line deletions in Argentine retinoblastoma patients.
    Fernández C, Repetto K, Dalamon V, Bergonzi F, Ferreiro V, Szijan I.
    Mol Diagn Ther; 2007 May; 11(1):55-61. PubMed ID: 17286450
    [Abstract] [Full Text] [Related]

  • 20. Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families.
    Goddard AD, Phillips RA, Greger V, Passarge E, Höpping W, Zhu XP, Gallie BL, Horsthemke B.
    Clin Genet; 1990 Feb; 37(2):117-26. PubMed ID: 1968790
    [Abstract] [Full Text] [Related]

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