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Journal Abstract Search

305 related items for PubMed ID: 11503314

  • 1. [From gene to disease; from SHOX to Lèri-Weill dyschondrosteosis, Turner syndrome and idiopathic short stature].
    Kant SG, Drop SL.
    Ned Tijdschr Geneeskd; 2001 Jul 28; 145(30):1456-9. PubMed ID: 11503314
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  • 2. Duplications upstream and downstream of SHOX identified as novel causes of Leri-Weill dyschondrosteosis or idiopathic short stature.
    Bunyan DJ, Baffico M, Capone L, Vannelli S, Iughetti L, Schmitt S, Taylor EJ, Herridge AA, Shears D, Forabosco A, Coviello DA.
    Am J Med Genet A; 2016 Apr 28; 170A(4):949-57. PubMed ID: 26698168
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  • 3. SHOX: growth, Léri-Weill and Turner syndromes.
    Blaschke RJ, Rappold GA.
    Trends Endocrinol Metab; 2000 Aug 28; 11(6):227-30. PubMed ID: 10878753
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  • 6. SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome.
    Cormier-Daire V, Belin V, Cusin V, Viot G, Girlich D, Toutain A, Moncla A, Vekemans M, Le Merrer M, Munnich A.
    Acta Paediatr Suppl; 1999 Dec 28; 88(433):55-9. PubMed ID: 10626546
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  • 12. Radiological signs of Leri-Weill dyschondrosteosis in Turner syndrome.
    Binder G, Fritsch H, Schweizer R, Ranke MB.
    Horm Res; 2001 Dec 28; 55(2):71-6. PubMed ID: 11509862
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  • 18. Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature.
    Rappold GA, Fukami M, Niesler B, Schiller S, Zumkeller W, Bettendorf M, Heinrich U, Vlachopapadoupoulou E, Reinehr T, Onigata K, Ogata T.
    J Clin Endocrinol Metab; 2002 Mar 28; 87(3):1402-6. PubMed ID: 11889216
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