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Journal Abstract Search

161 related items for PubMed ID: 2883107

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  • 2. 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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  • 3. 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; 80(2):177-80. PubMed ID: 2902000
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  • 4. Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome).
    MacDermot KD, Winter RM, Malcolm S.
    Hum Genet; 1986 Oct; 74(2):172-3. PubMed ID: 3464559
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  • 5. 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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  • 7. Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasia.
    Goodship J, Malcolm S, Clarke A, Pembrey ME.
    J Med Genet; 1990 Jul; 27(7):422-5. PubMed ID: 2395159
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  • 8. Hypohidrotic ectodermal dysplasia: argument against an autosomal recessive form clinically indistinguishable from X-linked hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome).
    Sybert VP.
    Pediatr Dermatol; 1989 Jun; 6(2):76-81. PubMed ID: 2748478
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  • 9. Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12.
    Kølvraa S, Kruse TA, Jensen PK, Linde KH, Vestergaard SR, Bolund L.
    Hum Genet; 1986 Nov; 74(3):284-7. PubMed ID: 2877938
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  • 10. Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder.
    Munoz F, Lestringant G, Sybert V, Frydman M, Alswaini A, Frossard PM, Jorgenson R, Zonana J.
    Am J Hum Genet; 1997 Jul; 61(1):94-100. PubMed ID: 9245989
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  • 11. Choroideremia-locus maps between DXS3 and DXS11 on Xq.
    Gal A, Brunsmann F, Hogenkamp D, Rüther K, Ahlert D, Wienker TF, Hammerstein W, Pawlowitzki IH.
    Hum Genet; 1986 Jun; 73(2):123-6. PubMed ID: 3755117
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  • 13. Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis.
    Zonana J, Schinzel A, Upadhyaya M, Thomas NS, Anton-Lamprecht I, Harper PS.
    Am J Med Genet; 1990 Jan; 35(1):132-5. PubMed ID: 2301463
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  • 15. A linkage study of the locus for X-linked Charcot-Marie-Tooth disease.
    Goonewardena P, Welihinda J, Anvret M, Gyftodimou J, Haegermark A, Iselius L, Lindsten J, Pettersson U.
    Clin Genet; 1988 Jun; 33(6):435-40. PubMed ID: 2901924
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  • 16. Linkage relationships of X-linked choroideremia to DXYS1 and DXS3.
    MacDonald IM, Sandre RM, Wong P, Hunter AG, Tenniswood MP.
    Hum Genet; 1987 Nov; 77(3):233-5. PubMed ID: 2890569
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