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253 related items for PubMed ID: 12035792

  • 1. Trisomy of the short stature homeobox-containing gene (SHOX), resulting from a duplication-deletion of the X chromosome.
    Adamson KA, Cross I, Batch JA, Rappold GA, Glass IA, Ball SG.
    Clin Endocrinol (Oxf); 2002 May; 56(5):671-5. PubMed ID: 12035792
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  • 2. Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature.
    Del Rey G, Jasper H, Bengolea SV, Boywitt A, De Bellis R, Heinrich JJ.
    Horm Res Paediatr; 2010 May; 74(4):297-304. PubMed ID: 20689243
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  • 3. Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature.
    Ogata T, Kosho T, Wakui K, Fukushima Y, Yoshimoto M, Miharu N.
    J Clin Endocrinol Metab; 2000 Aug; 85(8):2927-30. PubMed ID: 10946905
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  • 6. Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short stature.
    Musebeck J, Mohnike K, Beye P, Tönnies H, Neitzel H, Schnabel D, Grüters A, Wieacker PF, Stumm M.
    Eur J Pediatr; 2001 Sep; 160(9):561-5. PubMed ID: 11585080
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  • 7. SHOX intragenic microsatellite analysis in patients with short stature.
    Ezquieta B, Cueva E, Oliver A, Gracia R.
    J Pediatr Endocrinol Metab; 2002 Feb; 15(2):139-48. PubMed ID: 11874178
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  • 12. 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; 87(3):1402-6. PubMed ID: 11889216
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  • 13. The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.
    Clement-Jones M, Schiller S, Rao E, Blaschke RJ, Zuniga A, Zeller R, Robson SC, Binder G, Glass I, Strachan T, Lindsay S, Rappold GA.
    Hum Mol Genet; 2000 Mar 22; 9(5):695-702. PubMed ID: 10749976
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  • 14. [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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  • 16. Identification of short stature caused by SHOX defects and therapeutic effect of recombinant human growth hormone.
    Binder G, Schwarze CP, Ranke MB.
    J Clin Endocrinol Metab; 2000 Jan 28; 85(1):245-9. PubMed ID: 10634394
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