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

209 related items for PubMed ID: 4015485

  • 1. Retinoblastoma and retinoma occurring in a child with a translocation and deletion of the long arm of chromosome 13.
    Keith CG, Webb GC.
    Arch Ophthalmol; 1985 Jul; 103(7):941-4. PubMed ID: 4015485
    [Abstract] [Full Text] [Related]

  • 2. Deletion of 13q in two patients with retinoblastoma, one probably due to 13q-mosaicism in the mother.
    Michalová K, Kloucek F, Musilová J.
    Hum Genet; 1982 Jul; 61(3):264-6. PubMed ID: 7173873
    [Abstract] [Full Text] [Related]

  • 3. A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q.
    Motegi T, Kaga M, Yanagawa Y, Kadowaki H, Watanabe K, Inoue A, Komatsu M, Minoda K.
    Hum Genet; 1983 Jul; 64(2):160-2. PubMed ID: 6885051
    [Abstract] [Full Text] [Related]

  • 4. High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods).
    Motegi T.
    Hum Genet; 1982 Jul; 61(2):95-7. PubMed ID: 7129450
    [No Abstract] [Full Text] [Related]

  • 5. Retinoblastoma: host resistance and 13q- chromosomal deletion.
    Matsunaga E.
    Hum Genet; 1980 Jul; 56(1):53-8. PubMed ID: 7203480
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [A case of bilateral retinoblastoma with monosomy 13 (q12 leads to 114) (author's transl)].
    Walbaum R, François P, Farriaux JP, Woillez M.
    Hum Genet; 1978 Oct 31; 44(2):219-26. PubMed ID: 730167
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Retinoblastoma and subband deletion of chromosome 13.
    Yunis JJ, Ramsay N.
    Am J Dis Child; 1978 Feb 09; 132(2):161-3. PubMed ID: 626181
    [Abstract] [Full Text] [Related]

  • 10. Sporadic bilateral retinoblastoma and 13q- chromosomal deletion.
    Francke U, Kung F.
    Med Pediatr Oncol; 1976 Feb 09; 2(4):379-85. PubMed ID: 1004381
    [Abstract] [Full Text] [Related]

  • 11. Chromosomal anomalies in patients with retinoblastoma.
    Wilson MG, Ebbin AJ, Towner JW, Spencer WH.
    Clin Genet; 1977 Jul 09; 12(1):1-8. PubMed ID: 891004
    [Abstract] [Full Text] [Related]

  • 12. Bilateral retinoblastoma associated with 13q-mosaicism. Possible manifestation of a germinal mutation.
    Ribeiro MC, Andrade JA, Erwenne CM, Brunoni D.
    Cancer Genet Cytogenet; 1988 Jun 09; 32(2):169-75. PubMed ID: 3365680
    [Abstract] [Full Text] [Related]

  • 13. Retinoblastoma and chromosome abnormality. Partial deletion of the long arm of chromosome 13.
    Howard RO, Breg WR, Albert DM, Lesser RL.
    Arch Ophthalmol; 1974 Dec 09; 92(6):490-3. PubMed ID: 4433268
    [No Abstract] [Full Text] [Related]

  • 14. Constitutional karyotype in retinoblastoma. Case report and review of literature.
    Munier F, Pescia G, Jotterand-Bellomo M, Balmer A, Gailloud C, Thonney F.
    Ophthalmic Paediatr Genet; 1989 Jun 09; 10(2):129-50. PubMed ID: 2674826
    [Abstract] [Full Text] [Related]

  • 15. Hereditary retinoblastoma and 13q--mosaicism.
    Dudin G, Nasr A, Traboulsi E, Khouri F, Der Kaloustian VM.
    Cytogenet Cell Genet; 1984 Jun 09; 38(3):235-7. PubMed ID: 6336322
    [Abstract] [Full Text] [Related]

  • 16. 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 09; 3(3):243-50. PubMed ID: 7284985
    [Abstract] [Full Text] [Related]

  • 17. Retinoblastoma in a boy with a de novo mutation of a 13/18 translocation: the assumption that the retinoblastoma locus is at 13q141, particularly at the distal portion of it.
    Motegi T, Komatsu M, Nakazato Y, Ohuchi M, Minoda K.
    Hum Genet; 1982 Apr 09; 60(2):193-5. PubMed ID: 6985466
    [Abstract] [Full Text] [Related]

  • 18. De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.
    Calzolari E, Palazzi P, Aiello V, Mazzeo E, Perri P, Minelli A, del Senno L, Patracchini P, Bernardi F.
    Hum Genet; 1987 Sep 09; 77(1):51-4. PubMed ID: 3502696
    [Abstract] [Full Text] [Related]

  • 19. [Retinoblastoma and interstitial deletion of 13q (author's transl)].
    De Grouchy J, Turleau C, Cabanis MO, Richardet JM.
    Arch Fr Pediatr; 1980 Oct 09; 37(8):531-5. PubMed ID: 7447607
    [Abstract] [Full Text] [Related]

  • 20. Retinoblastoma. A model of hereditary fragile chromosomal regions.
    Hashem N, Khalifa S.
    Hum Hered; 1975 Oct 09; 25(1):35-49. PubMed ID: 1150293
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.