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Journal Abstract Search

214 related items for PubMed ID: 1550125

  • 1. Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1.
    Kupke KG, Graeber MB, Müller U.
    Am J Hum Genet; 1992 Apr; 50(4):808-15. PubMed ID: 1550125
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  • 2. Delineation of the dystonia-parkinsonism syndrome locus in Xq13.
    Graeber MB, Kupke KG, Müller U.
    Proc Natl Acad Sci U S A; 1992 Sep 01; 89(17):8245-8. PubMed ID: 1518853
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  • 3. DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3).
    Müller U, Haberhausen G, Wagner T, Fairweather ND, Chelly J, Monaco AP.
    Genomics; 1994 Sep 01; 23(1):114-7. PubMed ID: 7829058
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  • 4. Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome.
    Wilhelmsen KC, Weeks DE, Nygaard TG, Moskowitz CB, Rosales RL, dela Paz DC, Sobrevega EE, Fahn S, Gilliam TC.
    Ann Neurol; 1991 Feb 01; 29(2):124-31. PubMed ID: 1672807
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  • 6. Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3).
    Németh AH, Nolte D, Dunne E, Niemann S, Kostrzewa M, Peters U, Fraser E, Bochukova E, Butler R, Brown J, Cox RD, Levy ER, Ropers HH, Monaco AP, Müller U.
    Genomics; 1999 Sep 15; 60(3):320-9. PubMed ID: 10493831
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  • 7. Multipoint linkage analysis in Menkes disease.
    Tønnesen T, Petterson A, Kruse TA, Gerdes AM, Horn N.
    Am J Hum Genet; 1992 May 15; 50(5):1012-7. PubMed ID: 1570830
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  • 8. New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).
    Domingo A, Westenberger A, Lee LV, Brænne I, Liu T, Vater I, Rosales R, Jamora RD, Pasco PM, Cutiongco-Dela Paz EM, Freimann K, Schmidt TG, Dressler D, Kaiser FJ, Bertram L, Erdmann J, Lohmann K, Klein C.
    Eur J Hum Genet; 2015 Oct 15; 23(10):1334-40. PubMed ID: 25604858
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  • 9. Sex linked recessive dystonia parkinsonism of Panay, Philippines (XDP).
    Lee LV, Munoz EL, Tan KT, Reyes MT.
    Mol Pathol; 2001 Dec 15; 54(6):362-8. PubMed ID: 11724910
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  • 10. AFX1 and p54nrb: fine mapping, genomic structure, and exclusion as candidate genes of X-linked dystonia parkinsonism.
    Peters U, Haberhausen G, Kostrzewa M, Nolte D, Müller U.
    Hum Genet; 1997 Oct 15; 100(5-6):569-72. PubMed ID: 9341872
    [Abstract] [Full Text] [Related]

  • 11. Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1.
    Haberhausen G, Schmitt I, Köhler A, Peters U, Rider S, Chelly J, Terwilliger JD, Monaco AP, Müller U.
    Am J Hum Genet; 1995 Sep 15; 57(3):644-50. PubMed ID: 7668293
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  • 12. Gene for non-specific X-linked mental retardation maps in the pericentromeric region.
    Samanns C, Albrecht R, Neugebauer M, Neri G, Gal A.
    Am J Med Genet; 1991 Sep 15; 38(2-3):224-7. PubMed ID: 2018062
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  • 13. Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker.
    Hanauer A, Alembik Y, Arveiler B, Formiga L, Gilgenkrantz S, Mandel JL.
    Hum Genet; 1988 Oct 15; 80(2):177-80. PubMed ID: 2902000
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  • 16. The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21).
    Saugier-Veber P, Abadie V, Moncla A, Mathieu M, Piussan C, Turleau C, Mattei JF, Munnich A, Lyonnet S.
    Am J Hum Genet; 1993 Jun 15; 52(6):1040-5. PubMed ID: 8503439
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  • 19. X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.
    Zonana J, Clarke A, Sarfarazi M, Thomas NS, Roberts K, Marymee K, Harper PS.
    Am J Hum Genet; 1988 Jul 15; 43(1):75-85. PubMed ID: 3163892
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  • 20. Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male.
    Goodship J, Levinsky R, Malcolm S.
    Hum Genet; 1989 Dec 15; 84(1):11-4. PubMed ID: 2606471
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