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148 related items for PubMed ID: 10398240

  • 21. Characterization of ARHGEF6, a guanine nucleotide exchange factor for Rho GTPases and a candidate gene for X-linked mental retardation: mutation screening in Börjeson-Forssman-Lehmann syndrome and MRX27.
    Lower KM, Gecz J.
    Am J Med Genet; 2001 Apr 15; 100(1):43-8. PubMed ID: 11337747
    [Abstract] [Full Text] [Related]

  • 22. XLMR genes: update 1992.
    Neri G, Chiurazzi P, Arena F, Lubs HA, Glass IA.
    Am J Med Genet; 2001 Apr 15; 43(1-2):373-82. PubMed ID: 1605215
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  • 23. Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.
    Bach I, Robinson D, Thomas N, Ropers HH, Cremers FP.
    Hum Genet; 1992 Aug 15; 89(6):620-4. PubMed ID: 1511979
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  • 24. Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21.
    Badenas C, Castellví-Bel S, Volpini V, Jiménez D, Sánchez A, Estivill X, Milà M.
    Am J Med Genet; 2001 Feb 01; 98(4):343-7. PubMed ID: 11170079
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  • 25. Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26.
    Yntema HG, Hamel BC, Smits AP, van Roosmalen T, van den Helm B, Kremer H, Ropers HH, Smeets DF, van Bokhoven H.
    J Med Genet; 1998 Oct 01; 35(10):801-5. PubMed ID: 9783701
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  • 26. Construction of a highly annotated cosmid contig spanning 550Kb within the X-linked nonspecific mental retardation candidate region at Xp21.3-22.1.
    Carrié A, Nepotes V, Billuart P, Beldjord C, Bienvenu T, Chelly J, Bruls T, Heilig R, Weissenbach J, Jun L, Marynen P.
    Am J Med Genet; 1999 Jul 30; 85(3):252-4. PubMed ID: 10398238
    [No Abstract] [Full Text] [Related]

  • 27. Localisation of the MRX3 gene for non-specific X linked mental retardation.
    Gedeon A, Kerr B, Mulley J, Turner G.
    J Med Genet; 1991 Jun 30; 28(6):372-7. PubMed ID: 1870093
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  • 30. Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1.
    Claes S, Volcke P, Devriendt K, Holvoet M, Raeymaekers P, Cassiman JJ, Fryns JP.
    Am J Med Genet; 1999 Jul 30; 85(3):283-7. PubMed ID: 10398244
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  • 32. Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation.
    Lossi AM, Laugier-Anfossi F, Depetris D, Gecz J, Gedeon A, Kooy F, Schwartz C, Mattei MG, Croquette MF, Villard L.
    J Med Genet; 2002 Feb 30; 39(2):113-7. PubMed ID: 11836360
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  • 33. Non-specific X linked mental retardation.
    Kerr B, Turner G, Mulley J, Gedeon A, Partington M.
    J Med Genet; 1991 Jun 30; 28(6):378-82. PubMed ID: 1870094
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  • 34. The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR).
    Van Buggenhout GJ, Trommelen JC, Brunner HG, Hamel BC, Fryns J.
    Ann Genet; 2001 Jun 30; 44(1):47-55. PubMed ID: 11334618
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  • 35. X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region.
    Yntema HG, van den Helm B, Knoers NV, Smits AP, van Roosmalen T, Smeets DF, Mariman EC, van der Burgt I, van Bokhoven H, Ropers HH, Kremer H, Hamel BC.
    Am J Med Genet; 1999 Jul 30; 85(3):305-8. PubMed ID: 10398247
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  • 37. Novel X-linked mental retardation syndrome with short stature maps to Xq24.
    Vitale E, Specchia C, Devoto M, Angius A, Rong S, Rocchi M, Schwalb M, Demelas L, Paglietti D, Manca S, Mastropaolo C, Serra G.
    Am J Med Genet; 2001 Sep 15; 103(1):1-8. PubMed ID: 11562927
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  • 40. A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation.
    Fukami M, Kirsch S, Schiller S, Richter A, Benes V, Franco B, Muroya K, Rao E, Merker S, Niesler B, Ballabio A, Ansorge W, Ogata T, Rappold GA.
    Am J Hum Genet; 2000 Sep 15; 67(3):563-73. PubMed ID: 10903929
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