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

148 related items for PubMed ID: 477414

  • 21. Cellular studies on retinoblastoma.
    Morten JE.
    Int J Radiat Biol Relat Stud Phys Chem Med; 1986 Mar; 49(3):485-93. PubMed ID: 2937750
    [Abstract] [Full Text] [Related]

  • 22. [Studies on deletions on chromosome 13 and their transmission in patients with retinoblastoma].
    Gao Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1991 Jun; 13(3):157-60. PubMed ID: 1831719
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. Deletions of the esterase D locus from a survey of 200 retinoblastoma patients.
    Cowell JK, Rutland P, Jay M, Hungerford J.
    Hum Genet; 1986 Feb; 72(2):164-7. PubMed ID: 3943870
    [Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26. A deleted chromosome no. 13 in human retinoblastoma cells: relevance to tumorigenesis.
    Balaban-Malenbaum G, Gilbert F, Nichols WW, Hill R, Shields J, Meadows AT.
    Cancer Genet Cytogenet; 1981 Apr; 3(3):243-50. PubMed ID: 7284985
    [Abstract] [Full Text] [Related]

  • 27. Retinoblastoma and subband deletion of chromosome 13.
    Yunis JJ, Ramsay N.
    Am J Dis Child; 1978 Feb; 132(2):161-3. PubMed ID: 626181
    [Abstract] [Full Text] [Related]

  • 28. The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions.
    Cowell JK, Thompson E, Rutland P.
    Arch Dis Child; 1987 Jan; 62(1):8-11. PubMed ID: 3813643
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus.
    Ward P, Packman S, Loughman W, Sparkes M, Sparkes R, McMahon A, Gregory T, Ablin A.
    J Med Genet; 1984 Apr; 21(2):92-5. PubMed ID: 6716423
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Gene carrier detection in retinoblastoma.
    Gallie BL.
    Ophthalmology; 1980 Jun; 87(6):591-5. PubMed ID: 7413148
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus.
    Horsthemke B, Greger V, Barnert HJ, Höpping W, Passarge E.
    Hum Genet; 1987 Jul; 76(3):257-61. PubMed ID: 2885256
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Retinoblastoma, gross internal malformations, and deletion 13q14 leads to q31.
    Yunis E, Zuñiga R, Ramírez E.
    Hum Genet; 1981 Jul; 56(3):283-6. PubMed ID: 7239512
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. [Hereditary tumors and chromosome aberrations with special reference to retinoblastoma].
    Sasaki MS.
    Gan To Kagaku Ryoho; 1986 Mar; 13(3 Pt 2):645-51. PubMed ID: 3963835
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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