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Journal Abstract Search

130 related items for PubMed ID: 9254866

  • 1. Evidence of a third locus in X-linked recessive spastic paraplegia.
    Steinmüller R, Lantigua-Cruz A, Garcia-Garcia R, Kostrzewa M, Steinberger D, Müller U.
    Hum Genet; 1997 Aug; 100(2):287-9. PubMed ID: 9254866
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  • 7. Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2.
    Tamagaki A, Shima M, Tomita R, Okumura M, Shibata M, Morichika S, Kurahashi H, Giddings JC, Yoshioka A, Yokobayashi Y.
    Am J Med Genet; 2000 Sep 04; 94(1):5-8. PubMed ID: 10982474
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  • 8. 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 04; 3(8):1263-7. PubMed ID: 7987300
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  • 10. Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description.
    Klebe S, Durr A, Bouslam N, Grid D, Paternotte C, Depienne C, Hanein S, Bouhouche A, Elleuch N, Azzedine H, Poea-Guyon S, Forlani S, Denis E, Charon C, Hazan J, Brice A, Stevanin G.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Oct 05; 144B(7):854-61. PubMed ID: 17503452
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  • 13. Male neonatal death and progressive weakness and immune deficiency in females: an unknown X linked condition.
    Woods G, Black G, Norbury G.
    J Med Genet; 1995 Mar 05; 32(3):191-6. PubMed ID: 7783167
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  • 14. Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia.
    Cambi F, Tang XM, Cordray P, Fain PR, Keppen LD, Barker DF.
    Neurology; 1996 Apr 05; 46(4):1112-7. PubMed ID: 8780101
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  • 19. Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methods.
    Kobayashi H, Matise TC, Perlin MW, Marks HG, Hoffman EP.
    Hum Genet; 1995 May 05; 95(5):483-90. PubMed ID: 7759066
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  • 20. X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28.
    Fryns JP, Spaepen A, Cassiman JJ, van den Berghe H.
    J Med Genet; 1991 Jun 05; 28(6):429-31. PubMed ID: 1870106
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