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Journal Abstract Search

161 related items for PubMed ID: 10982473

  • 41. Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome).
    Watty A, Prieto F, Beneyto M, Neugebauer M, Gal A.
    Am J Med Genet; 1991; 38(2-3):234-9. PubMed ID: 1673297
    [Abstract] [Full Text] [Related]

  • 42. Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one family.
    Ronce N, Raynaud M, Toutain A, Moizard MP, Colleaux L, Gendrot C, Briault S, Moraine C.
    Am J Med Genet; 1999 Mar 12; 83(2):132-7. PubMed ID: 10190484
    [Abstract] [Full Text] [Related]

  • 43. Allan-Herndon syndrome. I. Clinical studies.
    Stevenson RE, Goodman HO, Schwartz CE, Simensen RJ, McLean WT, Herndon CN.
    Am J Hum Genet; 1990 Sep 12; 47(3):446-53. PubMed ID: 2393019
    [Abstract] [Full Text] [Related]

  • 44. MASA syndrome: further clinical delineation and chromosomal localisation.
    Winter RM, Davies KE, Bell MV, Huson SM, Patterson MN.
    Hum Genet; 1989 Jul 12; 82(4):367-70. PubMed ID: 2737668
    [Abstract] [Full Text] [Related]

  • 45. Linkage analysis suggests at least two loci for X-linked non-specific mental retardation.
    Arveiler B, Alembik Y, Hanauer A, Jacobs P, Tranebjaerg L, Mikkelsen M, Puissant H, Piet LL, Mandel JL.
    Am J Med Genet; 1988 Jul 12; 30(1-2):473-83. PubMed ID: 3177465
    [Abstract] [Full Text] [Related]

  • 46. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q.
    Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J.
    Nat Genet; 1993 Oct 12; 5(2):163-7. PubMed ID: 8252041
    [Abstract] [Full Text] [Related]

  • 47. Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian family.
    Russo S, Cogliati F, Cavalleri F, Cassitto MG, Giglioli R, Toniolo D, Casari G, Larizza L.
    Am J Med Genet; 2000 Oct 23; 94(5):376-82. PubMed ID: 11050621
    [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 23; 34(7):529-34. PubMed ID: 9222958
    [Abstract] [Full Text] [Related]

  • 49. MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families.
    Schrander-Stumpel C, Fryns J, Cassiman JJ, Legius E, Spaepen A, Höweler CJ.
    J Med Genet; 1992 Mar 23; 29(3):215. PubMed ID: 1552562
    [No Abstract] [Full Text] [Related]

  • 50. Hereditary spastic diplegia with mental retardation in two young siblings.
    Gustavson KH, Modrzewska K, Erikson A.
    Clin Genet; 1989 Dec 23; 36(6):439-41. PubMed ID: 2591069
    [Abstract] [Full Text] [Related]

  • 51. Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21.
    Häne B, Schroer RJ, Arena JF, Lubs HA, Schwartz CE, Stevenson RE.
    Clin Genet; 1996 Oct 23; 50(4):176-83. PubMed ID: 9001795
    [Abstract] [Full Text] [Related]

  • 52. New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1.
    Orlacchio A, Kawarai T, Gaudiello F, St George-Hyslop PH, Floris R, Bernardi G.
    Ann Neurol; 2005 Sep 23; 58(3):423-9. PubMed ID: 16130112
    [Abstract] [Full Text] [Related]

  • 53. Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.
    Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dubé MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, Pericak-Vance MA, Raskind W, Rouleau GA, Siddique T.
    Neurology; 1996 Jun 23; 46(6):1507-14. PubMed ID: 8649538
    [Abstract] [Full Text] [Related]

  • 54. Linkage studies of X-linked recessive spastic paraplegia using DNA probes.
    Kenwrick S, Ionasescu V, Ionasescu G, Searby C, King A, Dubowitz M, Davies KE.
    Hum Genet; 1986 Jul 23; 73(3):264-6. PubMed ID: 3460961
    [Abstract] [Full Text] [Related]

  • 55. 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 23; 35(10):801-5. PubMed ID: 9783701
    [Abstract] [Full Text] [Related]

  • 56. Mental deficiency in three families with SPG4 spastic paraplegia.
    Ribaï P, Depienne C, Fedirko E, Jothy AC, Viveweger C, Hahn-Barma V, Brice A, Durr A.
    Eur J Hum Genet; 2008 Jan 23; 16(1):97-104. PubMed ID: 17957230
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  • 60. Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci.
    Patel H, Hart PE, Warner T, Allen I, Phillimore HE, Silver JR, Wood NW, Jeffery S, Patton MA, Crosby AH.
    Am J Med Genet; 2001 Jul 22; 102(1):68-72. PubMed ID: 11471175
    [Abstract] [Full Text] [Related]

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