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Journal Abstract Search

215 related items for PubMed ID: 7287000

  • 1. Lymphocyte chromosome survey in 42 patients with retinoblastoma: effort to detect 13q14 deletion mosaicism.
    Motegi T.
    Hum Genet; 1981; 58(2):168-73. PubMed ID: 7287000
    [Abstract] [Full Text] [Related]

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

  • 3. A decreasing tendency for cytogenetic abnormality in peripheral lymphocytes of retinoblastoma patients with 13q14 deletion mosaicism.
    Motegi T, Minoda K.
    Hum Genet; 1984; 66(2-3):186-9. PubMed ID: 6714979
    [Abstract] [Full Text] [Related]

  • 4. A case report of a patient with retinoblastoma and chromosome 13q deletion: assignment of a new gene (gene for LCP1) on human chromosome 13.
    Kondo I, Shin K, Honmura S, Nakajima H, Yamamura E, Satoh H, Terauchi M, Usuki Y, Takita H, Hamaguchi H.
    Hum Genet; 1985; 71(3):263-6. PubMed ID: 3864729
    [Abstract] [Full Text] [Related]

  • 5. Incidence and significance of a deletion of chromosome band 13q14 in patients with retinoblastoma and in their families.
    Liberfarb RM, Bustos T, Miller WA, Sang D.
    Ophthalmology; 1984 Dec; 91(12):1695-9. PubMed ID: 6521998
    [Abstract] [Full Text] [Related]

  • 6. 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 Dec; 61(3):264-6. PubMed ID: 7173873
    [Abstract] [Full Text] [Related]

  • 7. A genetic study of retinoblastoma.
    Liu XX, Sun YJ, Zhang L.
    J Tongji Med Univ; 1991 Dec; 11(4):220-4. PubMed ID: 1819032
    [Abstract] [Full Text] [Related]

  • 8. Familial retinoblastoma (mother and son) with 13q14 deletion.
    Fukushima Y, Kuroki Y, Ito T, Kondo I, Nishigaki I.
    Hum Genet; 1987 Oct; 77(2):104-7. PubMed ID: 3653883
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Lymphocyte chromosome survey in 80 patients with retinoblastoma.
    Mao WS, Lin XH, Ma QY, Chen YZ, Zeng LH, Dai ZY.
    Yan Ke Xue Bao; 1989 Jun; 5(1-2):7-13. PubMed ID: 2485748
    [Abstract] [Full Text] [Related]

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

  • 12. 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; 10(2):129-50. PubMed ID: 2674826
    [Abstract] [Full Text] [Related]

  • 13. 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; 32(2):169-75. PubMed ID: 3365680
    [Abstract] [Full Text] [Related]

  • 14. 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; 6(3):213-21. PubMed ID: 7116319
    [Abstract] [Full Text] [Related]

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

  • 17. Diagnosis of retinoblastoma in a presymptomatic stage after detection of interstitial chromosomal deletion 13q.
    Kennerknecht I, Barbi G, Greher J.
    Ophthalmic Genet; 1994 Mar; 15(1):19-24. PubMed ID: 7953248
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