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Journal Abstract Search

402 related items for PubMed ID: 8099916

  • 1. Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.
    Scheinman SJ, Pook MA, Wooding C, Pang JT, Frymoyer PA, Thakker RV.
    J Clin Invest; 1993 Jun; 91(6):2351-7. PubMed ID: 8099916
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  • 6. Evidence for a new locus for X-linked retinitis pigmentosa (RP23).
    Hardcastle AJ, Thiselton DL, Zito I, Ebenezer N, Mah TS, Gorin MB, Bhattacharya SS.
    Invest Ophthalmol Vis Sci; 2000 Jul; 41(8):2080-6. PubMed ID: 10892847
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  • 11. X-linked mental retardation with heterozygous expression and macrocephaly: pericentromeric gene localization.
    Turner G, Gedeon A, Mulley J.
    Am J Med Genet; 1994 Jul 15; 51(4):575-80. PubMed ID: 7943042
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  • 13. A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26.
    Priest JM, Fischbeck KH, Nouri N, Keats BJ.
    Genomics; 1995 Sep 20; 29(2):409-12. PubMed ID: 8666389
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  • 14. Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.
    Wolf MT, Zalewski I, Martin FC, Ruf R, Müller D, Hennies HC, Schwarz S, Panther F, Attanasio M, Acosta HG, Imm A, Lucke B, Utsch B, Otto E, Nurnberg P, Nieto VG, Hildebrandt F.
    Nephrol Dial Transplant; 2005 May 20; 20(5):909-14. PubMed ID: 15741201
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  • 15. X-linked recessive nephrolithiasis with renal failure.
    Frymoyer PA, Scheinman SJ, Dunham PB, Jones DB, Hueber P, Schroeder ET.
    N Engl J Med; 1991 Sep 05; 325(10):681-6. PubMed ID: 1908057
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  • 17. Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).
    Claes S, Vogels A, Holvoet M, Devriendt K, Raeymaekers P, Cassiman JJ, Fryns JP.
    Am J Med Genet; 1997 Dec 31; 73(4):474-9. PubMed ID: 9415477
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