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

103 related items for PubMed ID: 8946171

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

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

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

  • 4. Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family.
    Bürger J, Metzke H, Paternotte C, Schilling F, Hazan J, Reis A.
    Hum Genet; 1996 Sep; 98(3):371-5. PubMed ID: 8707310
    [Abstract] [Full Text] [Related]

  • 5. Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.
    Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung WY, Boustany RM, Bohlega S.
    Hum Mol Genet; 1994 Oct; 3(10):1867-71. PubMed ID: 7849714
    [Abstract] [Full Text] [Related]

  • 6. Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2.
    Raskind WH, Pericak-Vance MA, Lennon F, Wolff J, Lipe HP, Bird TD.
    Am J Med Genet; 1997 Feb 21; 74(1):26-36. PubMed ID: 9034002
    [Abstract] [Full Text] [Related]

  • 7. Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
    Scott WK, Gaskell PC, Lennon F, Wolpert CM, Menold MM, Aylsworth AS, Warner C, Farrell CD, Boustany RM, Albright SG, Boyd E, Kingston HM, Cumming WJ, Vance JM, Pericak-Vance MA.
    Neurogenetics; 1997 Sep 21; 1(2):95-102. PubMed ID: 10732810
    [Abstract] [Full Text] [Related]

  • 8. Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.
    Reid E, Dearlove AM, Whiteford ML, Rhodes M, Rubinsztein DC.
    Neurology; 1999 Nov 10; 53(8):1844-9. PubMed ID: 10563637
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 12. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
    Ashley-Koch A, Bonner ER, Gaskell PC, West SG, Tim R, Wolpert CM, Jones R, Farrell CD, Nance M, Svenson IK, Marchuk DA, Boustany RM, Vance JM, Scott WK, Pericak-Vance MA.
    Neurogenetics; 2001 Mar 10; 3(2):91-7. PubMed ID: 11354831
    [Abstract] [Full Text] [Related]

  • 13. 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 10; 30(5):381-4. PubMed ID: 8320699
    [Abstract] [Full Text] [Related]

  • 14. Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous trait.
    Dubé MP, Mlodzienski MA, Kibar Z, Farlow MR, Ebers G, Harper P, Kolodny EH, Rouleau GA, Figlewicz DA.
    Am J Hum Genet; 1997 Mar 10; 60(3):625-9. PubMed ID: 9042923
    [Abstract] [Full Text] [Related]

  • 15. Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3.
    Cruts M, Backhovens H, Theuns J, Clark RF, Le Paslier D, Weissenbach J, Goate AM, Martin JJ, Van Broeckhoven C.
    Hum Mol Genet; 1995 Aug 10; 4(8):1355-64. PubMed ID: 7581374
    [Abstract] [Full Text] [Related]

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

  • 17. Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.
    Dürr A, Davoine CS, Paternotte C, von Fellenberg J, Cogilinicean S, Coutinho P, Lamy C, Bourgeois S, Prud'homme JF, Penet C, Mas JL, Burgunder JM, Hazan J, Weissenbach J, Brice A, Fontaine B.
    Brain; 1996 Oct 10; 119 ( Pt 5)():1487-96. PubMed ID: 8931574
    [Abstract] [Full Text] [Related]

  • 18. Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2-q24.3.
    Huang S, Zhuyu, Li H, Labu, Baizhu, Lo WH, Fischer C, Vogel F.
    Hum Genet; 1997 Oct 10; 100(5-6):620-3. PubMed ID: 9341882
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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