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Journal Abstract Search

321 related items for PubMed ID: 9311732

  • 21. 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]

  • 22. [Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations].
    Nájera C, Sánchez F, Mateu E, Prieto F, Beneyto M.
    Med Clin (Barc); 2001 Mar 17; 116(10):365-72. PubMed ID: 11333669
    [Abstract] [Full Text] [Related]

  • 23. Constitutional deletions predisposing to retinoblastoma.
    Janson M, Kock E, Nordenskjöld M.
    Hum Genet; 1990 Jun 17; 85(1):21-4. PubMed ID: 1972694
    [Abstract] [Full Text] [Related]

  • 24. RB1 gene mutations in retinoblastoma.
    Lohmann DR.
    Hum Mutat; 1999 Jun 17; 14(4):283-8. PubMed ID: 10502774
    [Abstract] [Full Text] [Related]

  • 25. Mutational analysis of the RB1 gene in Indian patients with retinoblastoma.
    Ata-ur-Rasheed M, Vemuganti Gk, Honavar Sg, Ahmed N, Hasnain Se, Kannabiran C.
    Ophthalmic Genet; 2002 Jun 17; 23(2):121-8. PubMed ID: 12187430
    [Abstract] [Full Text] [Related]

  • 26.
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    [No Abstract] [Full Text] [Related]

  • 27. Preferential germline mutation of the paternal allele in retinoblastoma.
    Zhu XP, Dunn JM, Phillips RA, Goddard AD, Paton KE, Becker A, Gallie BL.
    Nature; 1989 Jul 27; 340(6231):312-3. PubMed ID: 2568588
    [Abstract] [Full Text] [Related]

  • 28. Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expression.
    Albrecht P, Ansperger-Rescher B, Schüler A, Zeschnigk M, Gallie B, Lohmann DR.
    Hum Mutat; 2005 Nov 27; 26(5):437-45. PubMed ID: 16127685
    [Abstract] [Full Text] [Related]

  • 29. A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families.
    Li WL, Buckley J, Sanchez-Lara PA, Maglinte DT, Viduetsky L, Tatarinova TV, Aparicio JG, Kim JW, Au M, Ostrow D, Lee TC, O'Gorman M, Judkins A, Cobrinik D, Triche TJ.
    J Mol Diagn; 2016 Jul 27; 18(4):480-93. PubMed ID: 27155049
    [Abstract] [Full Text] [Related]

  • 30. Constitutional retinoblastoma gene deletion in Egyptian patients.
    Mohammed AM, Kamel AK, Hammad SA, Afifi HH, El Sanabary Z, El Din ME.
    World J Pediatr; 2009 Aug 27; 5(3):222-5. PubMed ID: 19693468
    [Abstract] [Full Text] [Related]

  • 31. Age at diagnosis of isolated unilateral retinoblastoma does not distinguish patients with and without a constitutional RB1 gene mutation but is influenced by a parent-of-origin effect.
    Schüler A, Weber S, Neuhäuser M, Jurklies C, Lehnert T, Heimann H, Rudolph G, Jöckel KH, Bornfeld N, Lohmann DR.
    Eur J Cancer; 2005 Mar 27; 41(5):735-40. PubMed ID: 15763650
    [Abstract] [Full Text] [Related]

  • 32. RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling.
    Parma D, Ferrer M, Luce L, Giliberto F, Szijan I.
    PLoS One; 2017 Mar 27; 12(12):e0189736. PubMed ID: 29261756
    [Abstract] [Full Text] [Related]

  • 33. Loss of heterozygosity on chromosome 13 and its association with delayed growth of retinoblastoma.
    Kato MV, Ishizaki K, Ejima Y, Kaneko A, Tanooka H, Sasaki MS.
    Int J Cancer; 1993 Jul 30; 54(6):922-6. PubMed ID: 8335400
    [Abstract] [Full Text] [Related]

  • 34. [Retinoblastoma: clinical and molecular diagnostic aspects].
    Thonney F, Munier FL, Balmer A, Pescia G, Schorderet DF.
    Praxis (Bern 1994); 1996 Aug 27; 85(35):1058-62. PubMed ID: 8848678
    [Abstract] [Full Text] [Related]

  • 35. "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 Aug 27; 8():1. PubMed ID: 26753011
    [Abstract] [Full Text] [Related]

  • 36. Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma.
    Amare Kadam PS, Ghule P, Jose J, Bamne M, Kurkure P, Banavali S, Sarin R, Advani S.
    Cancer Genet Cytogenet; 2004 Apr 01; 150(1):33-43. PubMed ID: 15041221
    [Abstract] [Full Text] [Related]

  • 37. Genetics of retinoblastoma: a study.
    Mateu E, Sánchez F, Nájera C, Beneyto M, Castell V, Hernández M, Serra I, Prieto F.
    Cancer Genet Cytogenet; 1997 May 01; 95(1):40-50. PubMed ID: 9140452
    [Abstract] [Full Text] [Related]

  • 38. Age at diagnosis to discriminate those patients for whom constitutional DNA sequencing is appropriate in sporadic unilateral retinoblastoma.
    Zajaczek S, Jakubowska A, Kurzawski G, Krzystolik Z, Lubiński J.
    Eur J Cancer; 1998 Nov 01; 34(12):1919-21. PubMed ID: 10023315
    [Abstract] [Full Text] [Related]

  • 39. 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 Nov 01; 24():778-788. PubMed ID: 30636860
    [Abstract] [Full Text] [Related]

  • 40. [Molecular study of retinoblastoma in the Algerian population. Screening of Rb gene in constitutional and tumoral level].
    Boubekeur A, Louhibi L, Mahmoudi K, Boudjema A, Mehtar N.
    Bull Cancer; 2012 Feb 01; 99(2):127-35. PubMed ID: 22265791
    [Abstract] [Full Text] [Related]

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