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

188 related items for PubMed ID: 8045560

  • 21. Genetic heterogeneity in X-linked amelogenesis imperfecta.
    Aldred MJ, Crawford PJ, Roberts E, Gillespie CM, Thomas NS, Fenton I, Sandkuijl LA, Harper PS.
    Genomics; 1992 Nov; 14(3):567-73. PubMed ID: 1358807
    [Abstract] [Full Text] [Related]

  • 22. Linkage of an X-chromosome cleft palate gene.
    Moore GE, Ivens A, Chambers J, Farrall M, Williamson R, Page DC, Bjornsson A, Arnason A, Jensson O.
    Nature; 1992 Nov; 326(6108):91-2. PubMed ID: 2881212
    [Abstract] [Full Text] [Related]

  • 23. Linkage mapping of new X-linked juvenile retinoschisis kindreds using microsatellite markers.
    Shastry BS, Hejtmancik FJ, Margherio RT, Trese MT.
    Biochem Biophys Res Commun; 1996 Mar 27; 220(3):824-7. PubMed ID: 8607849
    [Abstract] [Full Text] [Related]

  • 24. Segregation analysis of cleft lip with or without cleft palate in the First Nations (Amerindian) people of British Columbia and review of isolated cleft palate etiologies.
    Lowry RB, Johnson CY, Gagnon F, Little J.
    Birth Defects Res A Clin Mol Teratol; 2009 Jun 27; 85(6):568-73. PubMed ID: 19215020
    [Abstract] [Full Text] [Related]

  • 25. The application of molecular genetics to detection of craniofacial abnormality.
    Moore G, Ivens A, Chambers J, Bjornsson A, Arnason A, Jensson O, Williamson R.
    Development; 1988 Jun 27; 103 Suppl():233-9. PubMed ID: 3074911
    [Abstract] [Full Text] [Related]

  • 26. Linkage analysis of a large pedigree with hereditary sideroblastic anaemia.
    Noble JS, Taylor GR, Losowsky MS, Hall R, Turner G, Mueller RF, Stewart AD.
    J Med Genet; 1995 May 27; 32(5):389-92. PubMed ID: 7616548
    [Abstract] [Full Text] [Related]

  • 27. 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 27; 84(21):7576-9. PubMed ID: 3478714
    [Abstract] [Full Text] [Related]

  • 28. Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigree.
    Sander A, Moser H, Liechti-Gallati S, Grimm T, Zingg M, Raveh J.
    Hum Genet; 1993 Mar 27; 91(1):55-62. PubMed ID: 8454288
    [Abstract] [Full Text] [Related]

  • 29. Sex-linked cleft palate in a British Columbia Indian family.
    Lowry RB.
    Pediatrics; 1970 Jul 27; 46(1):123-8. PubMed ID: 5423440
    [No Abstract] [Full Text] [Related]

  • 30. X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus.
    Bonneau D, Rozet JM, Bulteau C, Berthier M, Mettey R, Gil R, Munnich A, Le Merrer M.
    J Med Genet; 1993 May 27; 30(5):381-4. PubMed ID: 8320699
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations.
    Pauws E, Peskett E, Boissin C, Hoshino A, Mengrelis K, Carta E, Abruzzo MA, Lees M, Moore GE, Erickson RP, Stanier P.
    Clin Genet; 2013 Apr 27; 83(4):352-8. PubMed ID: 22784330
    [Abstract] [Full Text] [Related]

  • 33. Linkage studies in a pedigree with Van der Woude syndrome.
    Wienker TF, Hudek G, Bissbort S, Mayerová A, Mauff G, Bender K.
    J Med Genet; 1987 Mar 27; 24(3):160-2. PubMed ID: 3572998
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Multipoint linkage analysis in X-linked juvenile retinoschisis.
    Bergen AA, van Schooneveld MJ, Orth U, Bleeker-Wagemakers EM, Gal A.
    Clin Genet; 1993 Mar 27; 43(3):113-6. PubMed ID: 8500256
    [Abstract] [Full Text] [Related]

  • 36. Assignment of the X-linked torsion dystonia gene to Xq21 by linkage analysis.
    Kupke KG, Lee LV, Müller U.
    Neurology; 1990 Sep 27; 40(9):1438-42. PubMed ID: 1975433
    [Abstract] [Full Text] [Related]

  • 37. Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome.
    Peacocke M, Siminovitch KA.
    Proc Natl Acad Sci U S A; 1987 May 27; 84(10):3430-3. PubMed ID: 3472214
    [Abstract] [Full Text] [Related]

  • 38. Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus.
    Kwan SP, Terwilliger J, Parmley R, Raghu G, Sandkuyl LA, Ott J, Ochs H, Wedgwood R, Rosen F.
    Genomics; 1990 Feb 27; 6(2):238-42. PubMed ID: 2307467
    [Abstract] [Full Text] [Related]

  • 39. Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families.
    Wyszynski DF, Maestri N, McIntosh I, Smith EA, Lewanda AF, Garcia-Delgado C, Vinageras-Guarneros E, Wulfsberg E, Beaty TH.
    Hum Genet; 1997 Jan 27; 99(1):22-6. PubMed ID: 9003487
    [Abstract] [Full Text] [Related]

  • 40. Multipoint linkage mapping of the Xq25-q26 region in a family affected by the X-linked lymphoproliferative syndrome.
    Sylla BS, Wang Q, Hayoz D, Lathrop GM, Lenoir GM.
    Clin Genet; 1989 Dec 27; 36(6):459-62. PubMed ID: 2574086
    [Abstract] [Full Text] [Related]

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