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

185 related items for PubMed ID: 2569269

  • 1. Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene.
    Scheffer H, te Meerman GJ, Kruize YC, van den Berg AH, Penninga DP, Tan KE, der Kinderen DJ, Buys CH.
    Am J Hum Genet; 1989 Aug; 45(2):252-60. PubMed ID: 2569269
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma.
    Greger V, Kerst S, Messmer E, Höpping W, Passarge E, Horsthemke B.
    J Med Genet; 1988 Apr; 25(4):217-21. PubMed ID: 3163379
    [Abstract] [Full Text] [Related]

  • 6. [Prediction of retinoblastoma: linkage analysis of families with hereditary retinoblastoma by using polymorphic sites within the Rb gene].
    Yuan L, Gao Y, Lo S, Fang B, Ye J.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Oct; 17(5):338-42. PubMed ID: 8706167
    [Abstract] [Full Text] [Related]

  • 7. Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.
    Lohmann DR, Gerick M, Brandt B, Oelschläger U, Lorenz B, Passarge E, Horsthemke B.
    Am J Hum Genet; 1997 Aug; 61(2):282-94. PubMed ID: 9311732
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Accuracy of detection of the retinoblastoma gene by esterase D linkage.
    Halloran SL, Boughman JA, Dryja TP, Mukai S, Long D, Roberts DF, Craft AW.
    Arch Ophthalmol; 1985 Sep; 103(9):1329-31. PubMed ID: 3862370
    [Abstract] [Full Text] [Related]

  • 10. RB1 germ-line deletions in Argentine retinoblastoma patients.
    Fernández C, Repetto K, Dalamon V, Bergonzi F, Ferreiro V, Szijan I.
    Mol Diagn Ther; 2007 Sep; 11(1):55-61. PubMed ID: 17286450
    [Abstract] [Full Text] [Related]

  • 11. Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresis.
    Lohmann D, Horsthemke B, Gillessen-Kaesbach G, Stefani FH, Höfler H.
    Hum Genet; 1992 Apr; 89(1):49-53. PubMed ID: 1577465
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes.
    Haines JL, Ozelius L, St George-Hyslop P, Wexler NS, Gusella JF, Conneally PM.
    Genet Epidemiol; 1988 Apr; 5(6):375-80. PubMed ID: 2905314
    [Abstract] [Full Text] [Related]

  • 14. Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigrees.
    Munier FL, Wang MX, Spence MA, Thonney F, Balmer A, Pescia G, Donoso LA, Murphree AL.
    Arch Ophthalmol; 1993 Nov; 111(11):1507-11. PubMed ID: 8240106
    [Abstract] [Full Text] [Related]

  • 15. Exclusion of the retinoblastoma gene and chromosome 13q as the site of a primary lesion for human breast cancer.
    Bowcock AM, Hall JM, Hebert JM, King MC.
    Am J Hum Genet; 1990 Jan; 46(1):12-7. PubMed ID: 2294744
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Linkage of genes for human esterase D and hereditary retinoblastoma.
    Mukai S, Rapaport JM, Shields JA, Augsburger JJ, Dryja TP.
    Am J Ophthalmol; 1984 Jun; 97(6):681-5. PubMed ID: 6731533
    [Abstract] [Full Text] [Related]

  • 19. Family studies on the chromosomal location of the retinoblastoma gene (Rb-1).
    Morten J, Harnden DG, Bundey S.
    J Med Genet; 1982 Apr; 19(2):120-4. PubMed ID: 6951997
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.