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

175 related items for PubMed ID: 2883887

  • 1. Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.
    Lesko JG, Lewis RA, Nussbaum RL.
    Am J Hum Genet; 1987 Apr; 40(4):303-11. PubMed ID: 2883887
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Mapping X-linked ophthalmic diseases. Provisional assignment of the locus for choroideremia to Xq13-q24.
    Lewis RA, Nussbaum RL, Ferrell R.
    Ophthalmology; 1985 Jun; 92(6):800-6. PubMed ID: 4034175
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Linkage relationships of X-linked choroideremia to DXYS1 and DXS3.
    MacDonald IM, Sandre RM, Wong P, Hunter AG, Tenniswood MP.
    Hum Genet; 1987 Nov; 77(3):233-5. PubMed ID: 2890569
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome.
    Arveiler B, Oberlé I, Mandel JL.
    Genomics; 1987 Sep; 1(1):60-6. PubMed ID: 2889662
    [Abstract] [Full Text] [Related]

  • 9. X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.
    Zonana J, Clarke A, Sarfarazi M, Thomas NS, Roberts K, Marymee K, Harper PS.
    Am J Hum Genet; 1988 Jul; 43(1):75-85. PubMed ID: 3163892
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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]

  • 12. 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]

  • 13. 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]

  • 14. 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]

  • 15. Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion.
    Hodgson SV, Robertson ME, Fear CN, Goodship J, Malcolm S, Jay B, Bobrow M, Pembrey ME.
    Hum Genet; 1987 Mar; 75(3):286-90. PubMed ID: 3030927
    [Abstract] [Full Text] [Related]

  • 16. Gene mapping of X-linked choroideremia with restriction fragment-length polymorphisms.
    MacDonald IM, Sandre RM, Hunter AG, Tenniswood MP.
    Can J Ophthalmol; 1987 Oct; 22(6):310-5. PubMed ID: 2892583
    [Abstract] [Full Text] [Related]

  • 17. Deletion of the DXS165 locus in patients with classical choroideremia.
    Cremers FP, Brunsmann F, van de Pol TJ, Pawlowitzki IH, Paulsen K, Wieringa B, Ropers HH.
    Clin Genet; 1987 Dec; 32(6):421-3. PubMed ID: 3481306
    [Abstract] [Full Text] [Related]

  • 18. Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.
    de Saint Basile G, Arveiler B, Oberlé I, Malcolm S, Levinsky RJ, Lau YL, Hofker M, Debre M, Fischer A, Griscelli C.
    Proc Natl Acad Sci U S A; 1987 Nov; 84(21):7576-9. PubMed ID: 3478714
    [Abstract] [Full Text] [Related]

  • 19. Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation.
    Nussbaum RL, Lesko JG, Lewis RA, Ledbetter SA, Ledbetter DH.
    Proc Natl Acad Sci U S A; 1987 Sep; 84(18):6521-5. PubMed ID: 3476958
    [Abstract] [Full Text] [Related]

  • 20. Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.
    Musarella MA, Burghes A, Anson-Cartwright L, Mahtani MM, Argonza R, Tsui LC, Worton R.
    Am J Hum Genet; 1988 Oct; 43(4):484-94. PubMed ID: 2902787
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.