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Journal Abstract Search

120 related items for PubMed ID: 9736780

  • 21.
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  • 22. Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia.
    Bowen T, Guy CA, Cardno AG, Vincent JB, Kennedy JL, Jones LA, Gray M, Sanders RD, McCarthy G, Murphy KC, Owen MJ, O'Donovan MC.
    Psychiatr Genet; 2000 Mar; 10(1):33-7. PubMed ID: 10909126
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  • 25. Extensive genetic heterogeneity in the "pure" form of autosomal dominant familial spastic paraplegia (Strümpell's disease).
    Kobayashi H, Garcia CA, Tay PN, Hoffman EP.
    Muscle Nerve; 1996 Nov; 19(11):1435-8. PubMed ID: 8874401
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  • 26. Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.
    Gispert S, Santos N, Damen R, Voit T, Schulz J, Klockgether T, Orozco G, Kreuz F, Weissenbach J, Auburger G.
    Am J Hum Genet; 1995 Jan; 56(1):183-7. PubMed ID: 7825576
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  • 27. Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15.
    Martínez Murillo F, Kobayashi H, Pegoraro E, Galluzzi G, Creel G, Mariani C, Farina E, Ricci E, Alfonso G, Pauli RM, Hoffman EP.
    Neurology; 1999 Jul 13; 53(1):50-6. PubMed ID: 10408536
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  • 28. 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 13; 5(2):163-7. PubMed ID: 8252041
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  • 29. Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees.
    De Jonghe P, Krols L, Michalik A, Hazan J, Smeyers G, Löfgren A, Weissenbach J, Martin JJ, Van Broeckhoven C.
    Eur J Hum Genet; 1996 Oct 13; 4(5):260-6. PubMed ID: 8946171
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  • 31. A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array.
    Holmes SE, Wentzell JS, Seixas AI, Callahan C, Silveira I, Ross CA, Margolis RL.
    Hum Genet; 2006 Sep 13; 120(2):193-200. PubMed ID: 16783570
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  • 32. Spastic paraplegia, ataxia, mental retardation (SPAR): a novel genetic disorder.
    Hedera P, Rainier S, Zhao XP, Schalling M, Lindblad K, Yuan QP, Ikeuchi T, Trobe J, Wald JJ, Eldevik OP, Kluin K, Fink JK.
    Neurology; 2002 Feb 12; 58(3):411-6. PubMed ID: 11839840
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  • 35. Intergenerational CAG repeat expansion at ERDA1 in a family with childhood-onset depression, schizoaffective disorder, and recurrent major depression.
    Vincent JB, Kovacs M, Krol R, Barr CL, Kennedy JL.
    Am J Med Genet; 1999 Feb 05; 88(1):79-82. PubMed ID: 10050972
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  • 36. Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.
    Paternotte C, Rudnicki D, Fizames C, Davoine CS, Mavel D, Dürr A, Samson D, Marquette C, Muselet D, Vega-Czarny N, Drouot N, Voit T, Fontaine B, Gyapay G, Auburger G, Weissenbach J, Hazan J.
    Genome Res; 1998 Nov 05; 8(11):1216-27. PubMed ID: 9847083
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  • 39. Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2.
    Raskind WH, Pericak-Vance MA, Lennon F, Wolff J, Lipe HP, Bird TD.
    Am J Med Genet; 1997 Feb 21; 74(1):26-36. PubMed ID: 9034002
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  • 40. A CAG trinucleotide repeat expansion and familial schizophrenia.
    Ohara1 K, Ikeuchi T, Suzuki Y, Ohtani M, Ohara K, Tsuji S.
    Psychiatry Res; 2000 Jul 17; 94(3):257-62. PubMed ID: 10889290
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