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Journal Abstract Search

219 related items for PubMed ID: 1975433

  • 1.
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  • 2. The X-linked dystonia-parkinsonism syndrome (XDP): clinical and molecular genetic analysis.
    Graeber MB, Müller U.
    Brain Pathol; 1992 Oct; 2(4):287-95. PubMed ID: 1364136
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  • 3. Human gene for torsion dystonia located on chromosome 9q32-q34.
    Ozelius L, Kramer PL, Moskowitz CB, Kwiatkowski DJ, Brin MF, Bressman SB, Schuback DE, Falk CT, Risch N, de Leon D.
    Neuron; 1989 May; 2(5):1427-34. PubMed ID: 2576373
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  • 4. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21.
    Schwartz CE, Ulmer J, Brown A, Pancoast I, Goodman HO, Stevenson RE.
    Am J Hum Genet; 1990 Sep; 47(3):454-8. PubMed ID: 2393020
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  • 7. A study of idiopathic torsion dystonia in a non-Jewish family: evidence for genetic heterogeneity.
    Bressman SB, Heiman GA, Nygaard TG, Ozelius LJ, Hunt AL, Brin MF, Gordon MF, Moskowitz CB, de Leon D, Burke RE.
    Neurology; 1994 Feb; 44(2):283-7. PubMed ID: 8309575
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  • 10. Familial essential tremor and idiopathic torsion dystonia are different genetic entities.
    Dürr A, Stevanin G, Jedynak CP, Penet C, Agid Y, Brice A.
    Neurology; 1993 Nov; 43(11):2212-4. PubMed ID: 8232931
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  • 13. Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family.
    Thakker RV, Farmery MR, Sakati NA, Milner RD.
    Clin Endocrinol (Oxf); 1992 Oct; 37(4):338-43. PubMed ID: 1483289
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  • 14. Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus.
    Carpenter NJ, Thibodeau SN, Brown WT.
    Am J Med Genet; 1991 Oct; 38(2-3):349-53. PubMed ID: 1673310
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  • 15. X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region.
    Mostacciuolo ML, Müller E, Fardin P, Micaglio GF, Bardoni B, Guioli S, Camerino G, Danieli GA.
    Hum Genet; 1991 May; 87(1):23-7. PubMed ID: 1674715
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  • 17. Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA).
    Malcolm S, de Saint Basile G, Arveiler B, Lau YL, Szabo P, Fischer A, Griscelli C, Debre M, Mandel JL, Callard RE.
    Hum Genet; 1987 Oct; 77(2):172-4. PubMed ID: 2888720
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  • 18. Linkage analysis of the properdin deficiency gene: suggestion of a locus in the proximal part of the short arm of the X chromosome.
    Goonewardena P, Sjöholm AG, Nilsson LA, Pettersson U.
    Genomics; 1988 Feb; 2(2):115-8. PubMed ID: 2900806
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  • 19. Linkage of nonspecific X-linked mental retardation to Xq21.31.
    Jedele KB, Michels VV, Schaid DJ, Schowalter KV, Thibodeau SN.
    Am J Med Genet; 1988 Feb; 43(1-2):436-42. PubMed ID: 1605223
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  • 20. Linkage in a family with X-linked Charcot-Marie-Tooth disease.
    Haites N, Fairweather N, Clark C, Kelly KF, Simpson S, Johnston AW.
    Clin Genet; 1989 Jun; 35(6):399-403. PubMed ID: 2567643
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