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Journal Abstract Search

211 related items for PubMed ID: 2020294

  • 21. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
    Hedera P, Blair MA, Andermann E, Andermann F, D'Agostino D, Taylor KA, Chahine L, Pandolfo M, Bradford Y, Haines JL, Abou-Khalil B.
    Neurology; 2007 Jun 12; 68(24):2107-12. PubMed ID: 17377072
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  • 22. Gene linkage in familial amyotrophic lateral sclerosis: a progress report.
    Brown RH, Horvitz HR, Rouleau GA, McKenna-Yasek D, Beard C, Sapp P, Haines JL, Gusella JF, Figlewicz DA.
    Adv Neurol; 1991 Jun 12; 56():215-26. PubMed ID: 1853758
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  • 23. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.
    Orenstein SR, Shalaby TM, Finch R, Pfuetzer RH, DeVandry S, Chensny LJ, Bannada MM, Whitcomb DC.
    Am J Gastroenterol; 2002 Nov 12; 97(11):2725-32. PubMed ID: 12425539
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  • 28. Identification of flanking markers for the familial amyotrophic lateral sclerosis gene ALS1 on chromosome 21.
    Figlewicz DA, McInnis MG, Goto J, Haines JL, Warren AC, Krizus A, Khodr N, Brown RH, McKenna-Yasek D, Antonarakis SE.
    J Neurol Sci; 1994 Jul 12; 124 Suppl():90-5. PubMed ID: 7807155
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  • 29. Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.
    Chance PF, Rabin BA, Ryan SG, Ding Y, Scavina M, Crain B, Griffin JW, Cornblath DR.
    Am J Hum Genet; 1998 Mar 12; 62(3):633-40. PubMed ID: 9497266
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  • 32. Absence of linkage between chromosome 21 loci and familial amyotrophic lateral sclerosis.
    King A, Houlden H, Hardy J, Lane R, Chancellor A, de Belleroche J.
    J Med Genet; 1993 Apr 12; 30(4):318. PubMed ID: 8487280
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  • 33. More than one locus for familial amyotrophic lateral sclerosis: absence of linkage to the SMA locus.
    King AW, Orrell RW, Lane R, de Belleroche JS.
    Biochem Soc Trans; 1994 May 12; 22(2):149S. PubMed ID: 7958219
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  • 34. A first step toward a molecular genetic analysis of amyotrophic lateral sclerosis.
    Conneally PM.
    N Engl J Med; 1991 May 16; 324(20):1430-2. PubMed ID: 2020300
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  • 39. The gene encoding the glutamate receptor subunit GluR5 is located on human chromosome 21q21.1-22.1 in the vicinity of the gene for familial amyotrophic lateral sclerosis.
    Eubanks JH, Puranam RS, Kleckner NW, Bettler B, Heinemann SF, McNamara JO.
    Proc Natl Acad Sci U S A; 1993 Jan 01; 90(1):178-82. PubMed ID: 8419920
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