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Journal Abstract Search

148 related items for PubMed ID: 10398240

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42. Localization of MRX82: a new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family.
    Martínez F, Martínez-Garay I, Oltra S, Moltó MD, Orellana C, Monfort S, Prieto F, Tejada I.
    Am J Med Genet A; 2004 Dec 01; 131(2):174-8. PubMed ID: 15526294
    [Abstract] [Full Text] [Related]

  • 43. X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region.
    Gendrot C, Ronce N, Toutain A, Moizard MP, Müh JP, Raynaud M, Dourlens J, Briault S, Moraine C.
    Clin Genet; 1994 Mar 01; 45(3):145-53. PubMed ID: 8026106
    [Abstract] [Full Text] [Related]

  • 44.
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  • 45. Holmes-Gang syndrome is allelic with XLMR-hypotonic face syndrome.
    Stevenson RE, Abidi F, Schwartz CE, Lubs HA, Holmes LB.
    Am J Med Genet; 2000 Oct 23; 94(5):383-5. PubMed ID: 11050622
    [No Abstract] [Full Text] [Related]

  • 46. Refined gene localization for MRX7.
    Tackels D, Schwartz CE, Thibodeau SN, Michels VV.
    Am J Med Genet; 1999 Jul 30; 85(3):288-9. PubMed ID: 10398245
    [No Abstract] [Full Text] [Related]

  • 47. Refined gene localization for MRX8.
    Tackels D, Schwartz CE.
    Am J Med Genet; 1999 Jul 30; 85(3):309-10. PubMed ID: 10398248
    [No Abstract] [Full Text] [Related]

  • 48. A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28.
    Pai GS, Hane B, Joseph M, Nelson R, Hammond LS, Arena JF, Lubs HA, Stevenson RE, Schwartz CE.
    J Med Genet; 1997 Jul 30; 34(7):529-34. PubMed ID: 9222958
    [Abstract] [Full Text] [Related]

  • 49. Localization of a gene for nonspecific X-linked mental retardation (MRX 76) to Xp22.3-Xp21.3.
    Kleefstra T, Yntema HG, Oudakker AR, de Vries BB, van Bokhoven H, Hamel BC, Poppelaars FA, Ausems MG.
    Am J Med Genet; 2002 Jul 15; 110(4):410-1. PubMed ID: 12116222
    [No Abstract] [Full Text] [Related]

  • 50. Localization of non-specific X-linked mental retardation genes.
    Kerr B, Gedeon A, Mulley J, Turner G.
    Am J Med Genet; 2002 Jul 15; 43(1-2):392-401. PubMed ID: 1605217
    [Abstract] [Full Text] [Related]

  • 51. X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.
    Armfield K, Nelson R, Lubs HA, Häne B, Schroer RJ, Arena F, Schwartz CE, Stevenson RE.
    Am J Med Genet; 1999 Jul 30; 85(3):236-42. PubMed ID: 10398235
    [Abstract] [Full Text] [Related]

  • 52. Molecular study of the PAK3 and GDI1 genes in nonsyndromic X-linked mental retardation spanish patients.
    Rifé M, Mallolas J, Castellví-Bel S, Badenas C, Jiménez D, Milà M.
    Am J Med Genet; 2000 Oct 23; 94(5):389-91. PubMed ID: 11050624
    [No Abstract] [Full Text] [Related]

  • 53. Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three families.
    Lossi AM, Colleaux L, Chiaroni P, Fontes M, Villard L, Abidi F, Schwartz C, Briault S, Moraine C.
    Am J Med Genet; 2000 Oct 23; 94(5):386-8. PubMed ID: 11050623
    [No Abstract] [Full Text] [Related]

  • 54. 9th international workshop on fragile X syndrome and X-linked mental retardation.
    Fryns JP, Borghgraef M, Brown TW, Chelly J, Fisch GS, Hamel B, Hanauer A, Lacombe D, Luo L, MacPherson JN, Mandel JL, Moraine C, Mulley J, Nelson D, Oostra B, Partington M, Ramakers GJ, Ropers HH, Rousseau F, Schwartz C, Steinbach P, Stoll C, Tranebjaerg L, Turner G, Van Bokhoven H, Vianna-Morgante A.
    Am J Med Genet; 2000 Oct 23; 94(5):345-60. PubMed ID: 11050616
    [No Abstract] [Full Text] [Related]

  • 55. Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesity.
    Ahmad W, De Fusco M, Faiyaz ul Haque M, Aridon P, Sarno T, Sohail M, ul Haque S, Ahmad M, Ballabio A, Franco B, Casari G.
    Eur J Hum Genet; 1999 Oct 23; 7(7):828-32. PubMed ID: 10573017
    [Abstract] [Full Text] [Related]

  • 56. 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; 1999 Oct 23; 43(1-2):467-74. PubMed ID: 1605227
    [Abstract] [Full Text] [Related]

  • 57. Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).
    Gu XX, Decorte R, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P.
    J Med Genet; 1996 Jan 23; 33(1):52-5. PubMed ID: 8825049
    [Abstract] [Full Text] [Related]

  • 58. Rho proteins and the cellular mechanisms of mental retardation.
    Ramakers GJ.
    Am J Med Genet; 2000 Oct 23; 94(5):367-71. PubMed ID: 11050619
    [Abstract] [Full Text] [Related]

  • 59. X-linked mental retardation.
    Neri G, Chiurazzi P.
    Adv Genet; 1999 Oct 23; 41():55-94. PubMed ID: 10494617
    [No Abstract] [Full Text] [Related]

  • 60. Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHM.
    May M, Colleaux L, Murgia A, Aylsworth A, Nussbaum R, Fontes M, Schwartz C.
    Hum Mol Genet; 1995 Aug 23; 4(8):1465-6. PubMed ID: 7581391
    [No Abstract] [Full Text] [Related]

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