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Journal Abstract Search

214 related items for PubMed ID: 8474107

  • 1.
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  • 2. Further localization of X-linked hydrocephalus in the chromosomal region Xq28.
    Willems PJ, Vits L, Raeymaekers P, Beuten J, Coucke P, Holden JJ, Van Broeckhoven C, Warren ST, Sagi M, Robinson D.
    Am J Hum Genet; 1992 Aug; 51(2):307-15. PubMed ID: 1642232
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  • 4. The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52.
    Lyonnet S, Pelet A, Royer G, Delrieu O, Serville F, le Marec B, Gruensteudel A, Pfeiffer RA, Briard ML, Dubay C.
    Genomics; 1992 Oct; 14(2):508-10. PubMed ID: 1427869
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  • 5. Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families.
    Schrander-Stumpel C, Höweler C, Jones M, Sommer A, Stevens C, Tinschert S, Israel J, Fryns JP.
    Am J Med Genet; 1995 May 22; 57(1):107-16. PubMed ID: 7645588
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  • 6. 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 May 22; 5(1):1-10. PubMed ID: 8031529
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  • 7. X-linked hydrocephalus: clinical heterogeneity at a single gene locus.
    Serville F, Lyonnet S, Pelet A, Reynaud M, Louail C, Munnich A, Le Merrer M.
    Eur J Pediatr; 1992 Jul 22; 151(7):515-8. PubMed ID: 1396913
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  • 8. Fine mapping of X-linked clasped thumb and mental retardation (MASA syndrome) in Xq28.
    Legius E, Kaepernick L, Higgins JV, Glover TW.
    Clin Genet; 1994 Apr 22; 45(4):165-8. PubMed ID: 8062432
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  • 13. A duplication in the L1CAM gene associated with X-linked hydrocephalus.
    Van Camp G, Vits L, Coucke P, Lyonnet S, Schrander-Stumpel C, Darby J, Holden J, Munnich A, Willems PJ.
    Nat Genet; 1993 Aug 22; 4(4):421-5. PubMed ID: 8401593
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  • 14. Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.
    Yates JR, Warner JP, Smith JA, Deymeer F, Azulay JP, Hausmanowa-Petrusewicz I, Zaremba J, Borkowska J, Affara NA, Ferguson-Smith MA.
    J Med Genet; 1993 Feb 22; 30(2):108-11. PubMed ID: 8445613
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  • 16. Agenesis of the corpus callosum associated with MASA syndrome.
    Boyd E, Schwartz CE, Schroer RJ, May MM, Shapiro SD, Arena JF, Lubs HA, Stevenson RE.
    Clin Dysmorphol; 1993 Oct 22; 2(4):332-41. PubMed ID: 8305964
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  • 17. 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 22; 30(5):381-4. PubMed ID: 8320699
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  • 19. A novel L1CAM mutation with L1 spectrum disorders.
    Silan F, Ozdemir I, Lissens W.
    Prenat Diagn; 2005 Jan 22; 25(1):57-9. PubMed ID: 15662685
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  • 20. Linkage to Xq28 in a family with nonspecific X-linked mental retardation.
    Nordström AM, Penttinen M, von Koskull H.
    Hum Genet; 1992 Nov 22; 90(3):263-6. PubMed ID: 1362558
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