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Journal Abstract Search

161 related items for PubMed ID: 10982473

  • 1. Novel syndromic form of X-linked complicated spastic paraplegia.
    Claes S, Devriendt K, Van Goethem G, Roelen L, Meireleire J, Raeymaekers P, Cassiman JJ, Fryns JP.
    Am J Med Genet; 2000 Sep 04; 94(1):1-4. PubMed ID: 10982473
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  • 8. Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome.
    Arena JF, Schwartz C, Stevenson R, Lawrence L, Carpenter A, Duara R, Ledbetter D, Huang T, Lehner T, Ott J.
    Am J Med Genet; 2000 Sep 04; 43(1-2):479-90. PubMed ID: 1605230
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  • 10. Autosomal recessive spastic paraplegia (SPG45) with mental retardation maps to 10q24.3-q25.1.
    Dursun U, Koroglu C, Kocasoy Orhan E, Ugur SA, Tolun A.
    Neurogenetics; 2009 Oct 04; 10(4):325-31. PubMed ID: 19415352
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  • 12. Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24.
    des Portes V, Soufir N, Carrié A, Billuart P, Bienvenu T, Vinet MC, Beldjord C, Ponsot G, Kahn A, Boué J, Chelly J.
    Am J Med Genet; 1997 Oct 31; 72(3):324-8. PubMed ID: 9332663
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  • 13. The spectrum of "complicated spastic paraplegia, MASA syndrome and X-linked hydrocephalus". Contribution of DNA linkage analysis in genetic counseling of individual families.
    Schrander-Stumpel C, Meyer H, Merckx D, Jones M, Israel J, Sommer A, Stevens C, Tinschert S, Wilson G, Willems P.
    Genet Couns; 1994 Oct 31; 5(1):1-10. PubMed ID: 8031529
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  • 14. 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 31; 28(6):429-31. PubMed ID: 1870106
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  • 15. Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.
    Strain L, Wright AF, Bonthron DT.
    J Med Genet; 1997 Jul 31; 34(7):535-40. PubMed ID: 9222959
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  • 16. MRX8: an X-linked mental retardation condition with linkage to Xq21.
    Schwartz CE, May M, Huang T, Ledbetter D, Anderson G, Barker DF, Lubs HA, Arena F, Stevenson RE.
    Am J Med Genet; 1997 Jul 31; 43(1-2):467-74. PubMed ID: 1605227
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  • 17. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
    Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D.
    J Med Genet; 1995 Apr 31; 32(4):257-63. PubMed ID: 7643352
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  • 19. Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54).
    Jemaa LB, des Portes V, Zemni R, Mrad R, Maazoul F, Beldjord C, Chaabouni H, Chelly J.
    Am J Med Genet; 1999 Jul 30; 85(3):276-82. PubMed ID: 10398243
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