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Journal Abstract Search

165 related items for PubMed ID: 2904407

  • 1. Linkage studies in X-linked Alport's syndrome.
    Szpiro-Tapia S, Bobrie G, Guilloud-Bataille M, Heuertz S, Julier C, Frézal J, Grünfeld JP, Hors-Cayla MC.
    Hum Genet; 1988 Dec; 81(1):85-7. PubMed ID: 2904407
    [Abstract] [Full Text] [Related]

  • 2. Genetics of classic Alport's syndrome.
    Flinter FA, Cameron JS, Chantler C, Houston I, Bobrow M.
    Lancet; 1988 Oct 29; 2(8618):1005-7. PubMed ID: 2902439
    [Abstract] [Full Text] [Related]

  • 3. Multipoint linkage analysis in X-linked Alport syndrome.
    Hertz JM, Kruse TA, Thomsen A, Spencer ES.
    Hum Genet; 1991 Dec 29; 88(2):157-61. PubMed ID: 1684562
    [Abstract] [Full Text] [Related]

  • 4. Apparently changing patterns of inheritance in Alport's hereditary nephritis: genetic heterogeneity versus altered diagnostic criteria.
    Evans SH, Erickson RP, Kelsch R, Peirce JC.
    Clin Genet; 1980 Apr 29; 17(4):285-92. PubMed ID: 7371220
    [Abstract] [Full Text] [Related]

  • 5. Localization of the gene for X-linked Alport's syndrome.
    Brunner H, Schröder C, van Bennekom C, Lambermon E, Tuerlings J, Menzel D, Olbing H, Monnens L, Wieringa B, Ropers HH.
    Kidney Int; 1988 Oct 29; 34(4):507-10. PubMed ID: 3199669
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  • 7. Three new kindreds affected with Alport's syndrome.
    Barbera G, Costanzi S, Sturniolo A, Passalacqua S, Splendiani G, Sangiorgi M, Attanasio A, Capria A, Federico F.
    Contrib Nephrol; 1990 Oct 29; 80():143-6. PubMed ID: 2282814
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  • 9. Alport's syndrome: genetic evaluation of personal data concerning twelve families.
    Serbelloni P, Conte F, Gualandri V, Zanini M, Brambilla G, Pintucci JP, Sessa A.
    Contrib Nephrol; 1990 Oct 29; 80():126-30. PubMed ID: 2282810
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  • 11. Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndrome.
    Turco AE, Bresin E, Rossetti S, Peterlin B, Morandi R, Pignatti PF.
    Am J Kidney Dis; 1997 Aug 29; 30(2):174-9. PubMed ID: 9261027
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  • 14. Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.
    Saviranta P, Lindlöf M, Lehesjoki AE, Kalimo H, Lang H, Sonninen V, Savontaus ML, de la Chapelle A.
    Am J Hum Genet; 1988 Jan 29; 42(1):84-8. PubMed ID: 2892402
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  • 16. Autosomal dominant Alport's syndrome: study of a large Tunisian family.
    Kharrat M, Makni S, Makni K, Kammoun K, Charfeddine K, Azaeiz H, Jarraya F, Ben Hmida M, Gubler MC, Ayadi H, Hachicha J.
    Saudi J Kidney Dis Transpl; 2006 Sep 29; 17(3):320-5. PubMed ID: 16970251
    [Abstract] [Full Text] [Related]

  • 17. The inheritance of Alport's and related syndromes.
    Flinter FA, Bobrow M, Chantler C, Cameron JS.
    Nephrol Dial Transplant; 1990 Sep 29; 5(10):900. PubMed ID: 2128388
    [No Abstract] [Full Text] [Related]

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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 29; 90(3):316-8. PubMed ID: 1362559
    [Abstract] [Full Text] [Related]

  • 20. Genetic features of Alport's syndrome.
    Schröder CH, Brunner H, Monnens LA.
    Contrib Nephrol; 1990 Nov 29; 80():3-8. PubMed ID: 2282819
    [No Abstract] [Full Text] [Related]

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