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

101 related items for PubMed ID: 3481306

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 3. Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia.
    Schwartz M, Yang HM, Niebuhr E, Rosenberg T, Page DC.
    Hum Genet; 1988 Feb; 78(2):156-60. PubMed ID: 3422216
    [Abstract] [Full Text] [Related]

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

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Choroideremia in interstitial deletion of the X chromosome.
    Rosenberg T, Schwartz M, Niebuhr E, Yang HM, Sardemann H, Andersen O, Lundsteen C.
    Ophthalmic Paediatr Genet; 1986 Dec; 7(3):205-10. PubMed ID: 2882458
    [Abstract] [Full Text] [Related]

  • 7. Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical-genealogical evidence.
    Sankila EM, de la Chapelle A, Kärnä J, Forsius H, Frants R, Eriksson A.
    Clin Genet; 1987 May; 31(5):315-22. PubMed ID: 2886237
    [Abstract] [Full Text] [Related]

  • 8. Choroideremia-locus maps between DXS3 and DXS11 on Xq.
    Gal A, Brunsmann F, Hogenkamp D, Rüther K, Ahlert D, Wienker TF, Hammerstein W, Pawlowitzki IH.
    Hum Genet; 1986 Jun; 73(2):123-6. PubMed ID: 3755117
    [Abstract] [Full Text] [Related]

  • 9. Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.
    Nussbaum RL, Lewis RA, Lesko JG, Ferrell R.
    Am J Hum Genet; 1985 May; 37(3):473-81. PubMed ID: 2988333
    [Abstract] [Full Text] [Related]

  • 10. A genetic linkage study of choroideremia.
    Jay M, Wright AF, Clayton JF, Deans M, Dempster M, Bhattacharya SS, Jay B.
    Ophthalmic Paediatr Genet; 1986 Dec; 7(3):201-4. PubMed ID: 2882457
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Linkage studies and deletion screening in choroideremia.
    Wright AF, Nussbaum RL, Bhattacharya SS, Jay M, Lesko JG, Evans HJ, Jay B.
    J Med Genet; 1990 Aug; 27(8):496-8. PubMed ID: 1976814
    [Abstract] [Full Text] [Related]

  • 15. Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases.
    Cremers FP, Sankila EM, Brunsmann F, Jay M, Jay B, Wright A, Pinckers AJ, Schwartz M, van de Pol DJ, Wieringa B.
    Am J Hum Genet; 1990 Oct; 47(4):622-8. PubMed ID: 2220804
    [Abstract] [Full Text] [Related]

  • 16. Choroideremia, congenital deafness and mental retardation in a family with an X chromosomal deletion.
    Rosenberg T, Niebuhr E, Yang HM, Parving A, Schwartz M.
    Ophthalmic Paediatr Genet; 1987 Nov; 8(3):139-43. PubMed ID: 3438052
    [Abstract] [Full Text] [Related]

  • 17. Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.
    Cremers FP, van de Pol DJ, Diergaarde PJ, Wieringa B, Nussbaum RL, Schwartz M, Ropers HH.
    Genomics; 1989 Jan; 4(1):41-6. PubMed ID: 2914708
    [Abstract] [Full Text] [Related]

  • 18. Haplotype and multipoint linkage analysis in Finnish choroideremia families.
    Sankila EM, Lehner T, Eriksson AW, Forsius H, Kärnä J, Page D, Ott J, de la Chapelle A.
    Hum Genet; 1989 Dec; 84(1):66-70. PubMed ID: 2575071
    [Abstract] [Full Text] [Related]

  • 19. Choroideremia: further evidence for assignment of the locus to Xq13-Xq21.
    Schwartz M, Rosenberg T, Niebuhr E, Lundsteen C, Sardemann H, Andersen O, Yang HM, Lamm LU.
    Hum Genet; 1986 Dec; 74(4):449-52. PubMed ID: 2878872
    [Abstract] [Full Text] [Related]

  • 20. Choroideremia: linkage analysis with physically mapped close DNA-markers.
    Sankila EM, Sistonen P, Cremers F, de la Chapelle A.
    Hum Genet; 1991 Jul; 87(3):348-52. PubMed ID: 1677924
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.