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Journal Abstract Search

129 related items for PubMed ID: 7485266

  • 1. Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia.
    Speer MC, Kingston HM, Boustany RM, Gaskell PC, Robinson LC, Lennon F, Wolpert CM, Yamaoka LH, Kahler SG, Hogan EL.
    Am J Med Genet; 1995 Aug 14; 60(4):307-11. PubMed ID: 7485266
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  • 2. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q.
    Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J.
    Nat Genet; 1993 Oct 14; 5(2):163-7. PubMed ID: 8252041
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  • 3. Further evidence for a fourth gene causing X-linked pure spastic paraplegia.
    Starling A, Rocco P, Cambi F, Hobson GM, Passos Bueno MR, Zatz M.
    Am J Med Genet; 2002 Aug 01; 111(2):152-6. PubMed ID: 12210342
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  • 4. Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).
    Bouslam N, Benomar A, Azzedine H, Bouhouche A, Namekawa M, Klebe S, Charon C, Durr A, Ruberg M, Brice A, Yahyaoui M, Stevanin G.
    Ann Neurol; 2005 Apr 01; 57(4):567-71. PubMed ID: 15786464
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  • 6. Spastic paraplegia 15: linkage and clinical description of three Tunisian families.
    Boukhris A, Feki I, Denis E, Miladi MI, Brice A, Mhiri C, Stevanin G.
    Mov Disord; 2008 Feb 15; 23(3):429-33. PubMed ID: 18098276
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  • 10. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B.
    Mov Disord; 2006 Jan 15; 21(1):28-33. PubMed ID: 16124010
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  • 11. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
    Bruford EA, Riise R, Teague PW, Porter K, Thomson KL, Moore AT, Jay M, Warburg M, Schinzel A, Tommerup N, Tornqvist K, Rosenberg T, Patton M, Mansfield DC, Wright AF.
    Genomics; 1997 Apr 01; 41(1):93-9. PubMed ID: 9126487
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  • 12. A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia.
    Zhao GH, Hu ZM, Shen L, Jiang H, Ren ZJ, Liu XM, Xia K, Guo P, Pan Q, Tang BS.
    Chin Med J (Engl); 2008 Mar 05; 121(5):430-4. PubMed ID: 18364116
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  • 13. Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity.
    Lossos A, Stevanin G, Meiner V, Argov Z, Bouslam N, Newman JP, Gomori JM, Klebe S, Lerer I, Elleuch N, Silverstein S, Durr A, Abramsky O, Ben-Nariah Z, Brice A.
    Arch Neurol; 2006 May 05; 63(5):756-60. PubMed ID: 16682547
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  • 14. 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 05; 3(10):1867-71. PubMed ID: 7849714
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  • 16. Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity.
    Stöber G, Seelow D, Rüschendorf F, Ekici A, Beckmann H, Reis A.
    Hum Genet; 2002 Oct 05; 111(4-5):323-30. PubMed ID: 12384773
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  • 17. Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22.
    Anderson JL, Khan M, David WS, Mahdavi Z, Nuttall FQ, Krech E, West SG, Vance JM, Pericak-Vance MA, Nance MA.
    Am J Med Genet; 1999 Jan 15; 82(2):161-5. PubMed ID: 9934982
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  • 18. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.
    Rosen DR, Sapp P, O'Regan J, McKenna-Yasek D, Schlumpf KS, Haines JL, Gusella JF, Horvitz HR, Brown RH.
    Am J Med Genet; 1994 May 15; 51(1):61-9. PubMed ID: 7913294
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  • 19. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.
    Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T.
    Hum Mol Genet; 1994 Aug 15; 3(8):1263-7. PubMed ID: 7987300
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  • 20. Extensive genetic heterogeneity in the "pure" form of autosomal dominant familial spastic paraplegia (Strümpell's disease).
    Kobayashi H, Garcia CA, Tay PN, Hoffman EP.
    Muscle Nerve; 1996 Nov 15; 19(11):1435-8. PubMed ID: 8874401
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