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Journal Abstract Search

183 related items for PubMed ID: 10932263

  • 1. A gene for nonsyndromic mental retardation maps to chromosome 3p25-pter.
    Higgins JJ, Rosen DR, Loveless JM, Clyman JC, Grau MJ.
    Neurology; 2000 Aug 08; 55(3):335-40. PubMed ID: 10932263
    [Abstract] [Full Text] [Related]

  • 2. CALL gene is haploinsufficient in a 3p- syndrome patient.
    Angeloni D, Lindor NM, Pack S, Latif F, Wei MH, Lerman MI.
    Am J Med Genet; 1999 Oct 29; 86(5):482-5. PubMed ID: 10508992
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  • 4. Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity.
    Basel-Vanagaite L, Alkelai A, Straussberg R, Magal N, Inbar D, Mahajna M, Shohat M.
    J Med Genet; 2003 Oct 29; 40(10):729-32. PubMed ID: 14569116
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  • 6. Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant.
    Knight MA, Kennerson ML, Anney RJ, Matsuura T, Nicholson GA, Salimi-Tari P, Gardner RJ, Storey E, Forrest SM.
    Neurobiol Dis; 2003 Jul 29; 13(2):147-57. PubMed ID: 12828938
    [Abstract] [Full Text] [Related]

  • 7. Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33-q27.3.
    John P, Ali G, Chishti MS, Naqvi SM, Leal SM, Ahmad W.
    Hum Genet; 2006 Jan 29; 118(5):665-7. PubMed ID: 16273389
    [Abstract] [Full Text] [Related]

  • 8. Posterior column ataxia with retinitis pigmentosa (AXPC1) maps to chromosome 1q31-q32.
    Higgins JJ, Morton DH, Loveless JM.
    Neurology; 1999 Jan 01; 52(1):146-50. PubMed ID: 9921862
    [Abstract] [Full Text] [Related]

  • 9. 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
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  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2.
    Wali A, Ali G, John P, Lee K, Chishti MS, Leal SM, Ahmad W.
    Ann Hum Genet; 2007 Sep 30; 71(Pt 5):570-7. PubMed ID: 17451405
    [Abstract] [Full Text] [Related]

  • 12. Detailed mapping of a congenital heart disease gene in chromosome 3p25.
    Green EK, Priestley MD, Waters J, Maliszewska C, Latif F, Maher ER.
    J Med Genet; 2000 Aug 30; 37(8):581-7. PubMed ID: 10922384
    [Abstract] [Full Text] [Related]

  • 13. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
    Wong FK, Hagberg C, Karsten A, Larson O, Gustavsson M, Huggare J, Larsson C, Teh BT, Linder-Aronson S.
    Cleft Palate Craniofac J; 2000 Jul 30; 37(4):357-62. PubMed ID: 10912714
    [Abstract] [Full Text] [Related]

  • 14. Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric region.
    Holinski-Feder E, Chahrockh-Zadeh S, Rittinger O, Jedele KB, Gasteiger M, Lenski C, Murken J, Golla A.
    Am J Med Genet; 1999 Sep 10; 86(2):102-6. PubMed ID: 10449641
    [Abstract] [Full Text] [Related]

  • 15. A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2-q26.31.
    Wali A, John P, Gul A, Lee K, Chishti MS, Ali G, Hassan MJ, Leal SM, Ahmad W.
    Clin Genet; 2006 Sep 10; 70(3):233-9. PubMed ID: 16922726
    [Abstract] [Full Text] [Related]

  • 16. Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus.
    Dudding TE, Friend K, Schofield PW, Lee S, Wilkinson IA, Richards RI.
    Neurology; 2004 Dec 28; 63(12):2288-92. PubMed ID: 15623688
    [Abstract] [Full Text] [Related]

  • 17. Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.
    Martínez F, Martínez-Garay I, Millán JM, Pérez-Aytes A, Moltó MD, Orellana C, Prieto F.
    Am J Med Genet; 2001 Aug 01; 102(2):200-4. PubMed ID: 11477616
    [Abstract] [Full Text] [Related]

  • 18. Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping.
    Cormand B, Avela K, Pihko H, Santavuori P, Talim B, Topaloglu H, de la Chapelle A, Lehesjoki AE.
    Am J Hum Genet; 1999 Jan 01; 64(1):126-35. PubMed ID: 9915951
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 34(7):529-34. PubMed ID: 9222958
    [Abstract] [Full Text] [Related]

  • 20. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
    Ramprasad VL, Sripriya S, Ronnie G, Nancarrow D, Saxena S, Hemamalini A, Kumar D, Vijaya L, Kumaramanickavel G.
    Mol Vis; 2005 Nov 03; 11():934-40. PubMed ID: 16288197
    [Abstract] [Full Text] [Related]

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