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Journal Abstract Search

160 related items for PubMed ID: 2565084

  • 1. X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.
    Puck JM, Nussbaum RL, Smead DL, Conley ME.
    Am J Hum Genet; 1989 May; 44(5):724-30. PubMed ID: 2565084
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  • 2. Refinement of linkage of human severe combined immunodeficiency (SCIDX1) to polymorphic markers in Xq13.
    Puck JM, Conley ME, Bailey LC.
    Am J Hum Genet; 1993 Jul; 53(1):176-84. PubMed ID: 8317482
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  • 4. Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.
    de Saint Basile G, Arveiler B, Oberlé I, Malcolm S, Levinsky RJ, Lau YL, Hofker M, Debre M, Fischer A, Griscelli C.
    Proc Natl Acad Sci U S A; 1987 Nov; 84(21):7576-9. PubMed ID: 3478714
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  • 5. 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; 43(1):75-85. PubMed ID: 3163892
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  • 9. Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).
    Dahl N, Goonewardena P, Malmgren H, Gustavson KH, Holmgren G, Seemanova E, Annerén G, Flood A, Pettersson U.
    Am J Hum Genet; 1989 Aug; 45(2):304-9. PubMed ID: 2569270
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  • 10. X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus.
    Mensink EJ, Thompson A, Sandkuyl LA, Kraakman ME, Schot JD, Espanol T, Schuurman RK.
    Hum Genet; 1987 May; 76(1):96-9. PubMed ID: 2883112
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  • 12. 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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  • 13. Multipoint linkage analysis in Menkes disease.
    Tønnesen T, Petterson A, Kruse TA, Gerdes AM, Horn N.
    Am J Hum Genet; 1992 May; 50(5):1012-7. PubMed ID: 1570830
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  • 14. Genetic study of a new X-linked recessive immunodeficiency syndrome.
    de Saint-Basile G, Le Deist F, Caniglia M, Lebranchu Y, Griscelli C, Fischer A.
    J Clin Invest; 1992 Mar; 89(3):861-6. PubMed ID: 1347296
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  • 15. Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia.
    Schwartz M, Yang HM, Niebuhr E, Rosenberg T, Page DC.
    Hum Genet; 1988 Feb; 78(2):156-60. PubMed ID: 3422216
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  • 16. Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis.
    Zonana J, Sarfarazi M, Thomas NS, Clarke A, Marymee K, Harper PS.
    J Pediatr; 1989 Mar; 114(3):392-9. PubMed ID: 2564048
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  • 17. X chromosome linked immunodeficiency.
    Schwaber J, Rosen FS.
    Immunodefic Rev; 1990 Mar; 2(3):233-51. PubMed ID: 1981831
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  • 18. Prenatal diagnosis and genetic analysis of X-linked immunodeficiency disorders.
    Puck JM.
    Pediatr Res; 1993 Jan; 33(1 Suppl):S29-33; discussion S33-4. PubMed ID: 8433872
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  • 19. A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosome.
    Robinson D, Lamont M, Curtis G, Shields DC, Phelps P.
    Hum Genet; 1992 Nov; 90(3):316-8. PubMed ID: 1362559
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  • 20. Carrier detection of the X-linked primary immunodeficiency diseases using X-chromosome inactivation analysis.
    Winkelstein JA, Fearon E.
    J Allergy Clin Immunol; 1990 Jun; 85(6):1090-7. PubMed ID: 2191994
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