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Journal Abstract Search

167 related items for PubMed ID: 1349200

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  • 5. Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis.
    Stambolian D, Lewis RA, Buetow K, Bond A, Nussbaum R.
    Am J Hum Genet; 1990 Jul; 47(1):13-9. PubMed ID: 1971992
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  • 6. Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families.
    Thakker RV, Davies KE, Read AP, Tippett P, Wooding C, Flint T, Wood S, Kruse TA, Whyte MP, O'Riordan JL.
    Genomics; 1990 Oct; 8(2):189-93. PubMed ID: 1979046
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  • 8. The gene for spondyloepiphyseal dysplasia (SEDL) maps to Xp22 between DXS16 and DXS92.
    Heuertz S, Nelen M, Wilkie AO, Le Merrer M, Delrieu O, Larget-Piet L, Tranebjaerg L, Bick D, Hamel B, Van Oost BA.
    Genomics; 1993 Oct; 18(1):100-4. PubMed ID: 7903956
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  • 9. New markers for linkage analysis of X-linked hypophosphataemic rickets.
    Rowe PS, Goulding J, Read A, Mountford R, Hanauer A, Oudet C, Whyte MP, Meier-Ewert S, Lehrach H, Davies KE.
    Hum Genet; 1993 Jul; 91(6):571-5. PubMed ID: 8101831
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  • 10. A family with the Coffin Lowry syndrome revisited: localization of CLS to Xp21-pter.
    Partington MW, Mulley JC, Sutherland GR, Thode A, Turner G.
    Am J Med Genet; 1988 Jul; 30(1-2):509-21. PubMed ID: 3177468
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  • 11. Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region.
    Toutain A, Ronce N, Dessay B, Robb L, Francannet C, Le Merrer M, Briard ML, Kaplan J, Moraine C.
    Hum Genet; 1997 Feb; 99(2):256-61. PubMed ID: 9048931
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  • 15. Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region.
    Alitalo T, Kruse TA, Ahrens P, Albertsen HM, Eriksson AW, de la Chapelle A.
    Hum Genet; 1991 Apr; 86(6):599-603. PubMed ID: 1673960
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  • 16. Linkage mapping of a large Colombian family segregating for X linked retinoschisis: refinement of the chromosomal location.
    Shastry BS, Hejtmancik JF, Rodriguez A, Rodriguez F, Tamayo ML.
    J Med Genet; 1997 Jun; 34(6):504-6. PubMed ID: 9192273
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  • 17. An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS.
    Van de Vosse E, Bergen AA, Meershoek EJ, Oosterwijk JC, Gregory S, Bakker B, Weissenbach J, Coffey AJ, van Ommen GJ, Den Dunnen JT.
    Eur J Hum Genet; 1996 Jun; 4(2):101-4. PubMed ID: 8744027
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  • 18. Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.
    Martínez F, Martínez-Garay I, Millán JM, Pérez-Aytes A, Moltó MD, Orellana C, Prieto F.
    Am J Med Genet; 2001 Aug 01; 102(2):200-4. PubMed ID: 11477616
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  • 19. Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38).
    Schutz CK, Ives EJ, Chalifoux M, MacLaren L, Farrell S, Robinson PD, White BN, Holden JJ.
    Am J Med Genet; 1996 Jul 12; 64(1):89-96. PubMed ID: 8826457
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