These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

321 related items for 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
    [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 Aug; 33(1):53-61. PubMed ID: 23715307
    [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
    [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
    [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
    [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 Nov; 11(1):55-61. PubMed ID: 17286450
    [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
    [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
    [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
    [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
    [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
    [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
    [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 May; 9(3):200-11. PubMed ID: 16225399
    [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
    [Abstract] [Full Text] [Related]

  • 15. [Genetics of retinoblastoma].
    Minoda K.
    Nihon Rinsho; 1995 Nov; 53(11):2774-8. PubMed ID: 8538043
    [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 Nov; 4(2):93-9. PubMed ID: 18503160
    [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
    [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
    [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 Jul; 11(1):63-70. PubMed ID: 17286451
    [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 Jul; 59(4):248-52. PubMed ID: 1544317
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 17.