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Journal Abstract Search

148 related items for PubMed ID: 9737778

  • 1. Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22.
    Fischer J, Urtizberea JA, Pavek S, Vandiedonck C, Bruls T, Saker S, Alkatip Y, Prud'homme JF, Weissenbach J.
    Hum Genet; 1998 Jul; 103(1):60-4. PubMed ID: 9737778
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  • 2. Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene.
    el-Shanti H, Murray JC, Semina EV, Beutow KH, Scherpbier T, al-Alami J.
    Eur J Hum Genet; 1998 Jul; 6(3):251-6. PubMed ID: 9781029
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  • 3. Fine mapping of progressive pseudorheumatoid dysplasia: a tool for heterozygote identification.
    Alkhateeb A, al-Alami J, Leal SM, el-Shanti H.
    Genet Test; 1999 Jul; 3(4):329-33. PubMed ID: 10627939
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  • 4. Progressive pseudorheumatoid dysplasia: three cases in one family.
    Bennani L, Amine B, Ichchou L, Lazrak N, Hajjaj-Hassouni N.
    Joint Bone Spine; 2007 Jul; 74(4):393-5. PubMed ID: 17596985
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  • 5. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia.
    Iughetti P, Alonso LG, Wilcox W, Alonso N, Passos-Bueno MR.
    Am J Med Genet; 2000 Dec 18; 95(5):482-91. PubMed ID: 11146471
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  • 12. Localization of the gene for a novel autosomal recessive neurodegenerative Huntington-like disorder to 4p15.3.
    Kambouris M, Bohlega S, Al-Tahan A, Meyer BF.
    Am J Hum Genet; 2000 Feb 18; 66(2):445-52. PubMed ID: 10677304
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  • 13. Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval.
    Fontaine B, Nicole S, Topaloglu H, Ben Hamida C, Beighton P, Spaans F, Cantu JM, Bakouri S, Romero N, Ricker K, Barros-Nunez P, Ponsot G, Ben Hamida M, Weissenbach J, Hentati F, Lehmann-Horn F.
    Hum Genet; 1996 Sep 18; 98(3):380-5. PubMed ID: 8707312
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  • 17. Genetic mapping of Xp22.12-p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL).
    Heuertz S, Smahi A, Wilkie AO, Le Merrer M, Maroteaux P, Hors-Cayla MC.
    Hum Genet; 1995 Oct 18; 96(4):407-10. PubMed ID: 7557961
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  • 18. Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3.
    Faivre L, Le Merrer M, Al-Gazali LI, Ausems MG, Bitoun P, Bacq D, Maroteaux P, Munnich A, Cormier-Daire V.
    J Med Genet; 2003 Apr 18; 40(4):282-4. PubMed ID: 12676900
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