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

142 related items for PubMed ID: 7826849

  • 1. Outcome for patients with constitutional 13q chromosomal abnormalities and retinoblastoma.
    Pratt CB, Raimondi SC, Kaste SC, Heaton DM, Mounce KG, Mandrell B, Crom D, Meyer D.
    Pediatr Hematol Oncol; 1994; 11(5):541-7. PubMed ID: 7826849
    [Abstract] [Full Text] [Related]

  • 2. Failure to thrive leading to early detection of retinoblastoma.
    Kingston JE, Clark J, Santos H, Jones D, Hungerford JL.
    Pediatr Hematol Oncol; 1990; 7(2):199-203. PubMed ID: 2206862
    [No Abstract] [Full Text] [Related]

  • 3. Radiographic findings in 13q-syndrome.
    Kaste SC, Pratt CB.
    Pediatr Radiol; 1993; 23(7):545-8. PubMed ID: 8309761
    [Abstract] [Full Text] [Related]

  • 4. Chromosomal abnormalities in human retinoblastoma. A review.
    Potluri VR, Helson L, Ellsworth RM, Reid T, Gilbert F.
    Cancer; 1986 Aug 01; 58(3):663-71. PubMed ID: 3524791
    [Abstract] [Full Text] [Related]

  • 5. Retinoblastoma with 13q- chromosomal deletion associated with maternal paracentric inversion of 13q.
    Sparkes RS, Muller H, Klisak I.
    Science; 1979 Mar 09; 203(4384):1027-9. PubMed ID: 424728
    [Abstract] [Full Text] [Related]

  • 6. Frequency of 13q abnormalities among 203 patients with retinoblastoma.
    Bunin GR, Emanuel BS, Meadows AT, Buckley JD, Woods WG, Hammond GD.
    J Natl Cancer Inst; 1989 Mar 01; 81(5):370-4. PubMed ID: 2915374
    [Abstract] [Full Text] [Related]

  • 7. Retinoblastoma: clinical observations and histopathological study.
    Sang DN, Albert DM, Kuo PK.
    Int Ophthalmol Clin; 1982 Mar 01; 22(3):73-102. PubMed ID: 7107134
    [No Abstract] [Full Text] [Related]

  • 8. Complete or partial homozygosity of chromosome 13 in primary retinoblastoma.
    Benedict WF, Srivatsan ES, Mark C, Banerjee A, Sparkes RS, Murphree AL.
    Cancer Res; 1987 Aug 01; 47(15):4189-91. PubMed ID: 2886215
    [Abstract] [Full Text] [Related]

  • 9. Constitutional karyotypes in retinoblastoma.
    Turleau C, De Grouchy J.
    Ophthalmic Paediatr Genet; 1987 Mar 01; 8(1):11-7. PubMed ID: 3295639
    [Abstract] [Full Text] [Related]

  • 10. Tandem duplication (1) (q11----q22) in a male infant with multiple congenital malformations.
    Mertens F, Johansson B, Forslund M, Olsson M, Kristoffersson U.
    Clin Genet; 1987 Jul 01; 32(1):46-8. PubMed ID: 3621653
    [Abstract] [Full Text] [Related]

  • 11. Retinoblastoma and deletion of the long arm of chromosome 13: an underestimated diagnosis?
    Brichard B, Chantrain C, Gala JL, Sibille C, Vermylen C, De Potter P.
    Pediatr Blood Cancer; 2008 Mar 01; 50(3):694-6. PubMed ID: 16856159
    [Abstract] [Full Text] [Related]

  • 12. [Interstitial deletion of the long arms of chromosome 13].
    Molina M, Santolaya JM, Onaindía ML, Sánchez E, De Gárate J.
    An Esp Pediatr; 1982 Apr 01; 16(4):346-51. PubMed ID: 7125394
    [Abstract] [Full Text] [Related]

  • 13. Deletion (13)(q13q14.3) with retinoblastoma: confirmation and extension of a recognisable pattern of clinical features in retinoblastoma patients with 13q deletion.
    Motegi T, Ikeda K, Watanabe K, Yanagawa Y, Minoda K.
    J Med Genet; 1987 Nov 01; 24(11):696-7. PubMed ID: 3430545
    [Abstract] [Full Text] [Related]

  • 14. Retinoblastoma, chromosome abnormalities and oncogene expression.
    Gilbert F, Potluri VR, Short MP, Kau CL, Lalatta F.
    Ophthalmic Paediatr Genet; 1987 Mar 01; 8(1):3-10. PubMed ID: 3295640
    [Abstract] [Full Text] [Related]

  • 15. Chromosomal anomalies in patients with retinoblastoma.
    Wilson MG, Ebbin AJ, Towner JW, Spencer WH.
    Clin Genet; 1977 Jul 01; 12(1):1-8. PubMed ID: 891004
    [Abstract] [Full Text] [Related]

  • 16. Sporadic bilateral retinoblastoma and 13q- chromosomal deletion.
    Francke U, Kung F.
    Med Pediatr Oncol; 1976 Jul 01; 2(4):379-85. PubMed ID: 1004381
    [Abstract] [Full Text] [Related]

  • 17. Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes.
    Balaban G, Gilbert F, Nichols W, Meadows AT, Shields J.
    Cancer Genet Cytogenet; 1982 Jul 01; 6(3):213-21. PubMed ID: 7116319
    [Abstract] [Full Text] [Related]

  • 18. Familial pericentric inversion of chromosome 11 in a child with sporadic unilateral retinoblastoma.
    Ohnishi Y, Shigeto M, Ishibashi T, Hirata J.
    Ophthalmic Paediatr Genet; 1990 Dec 01; 11(4):281-5. PubMed ID: 2096356
    [Abstract] [Full Text] [Related]

  • 19. Chromosome 13 alterations in osteosarcoma cell lines derived from a patient with previous retinoblastoma.
    Hovig E, Lothe R, Farrants G, Brøgger A, Fodstad O, Børresen AL.
    Cancer Genet Cytogenet; 1991 Nov 01; 57(1):31-40. PubMed ID: 1684533
    [Abstract] [Full Text] [Related]

  • 20. Register of retinoblastoma: preliminary results.
    Jay M, Cowell J, Hungerford J.
    Eye (Lond); 1988 Nov 01; 2 ( Pt 1)():102-5. PubMed ID: 3410134
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.