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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

125 related items for PubMed ID: 3361200

  • 21.
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  • 22. Radiological signs of Leri-Weill dyschondrosteosis in Turner syndrome.
    Binder G, Fritsch H, Schweizer R, Ranke MB.
    Horm Res; 2001; 55(2):71-6. PubMed ID: 11509862
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  • 23. Carpal tunnel syndrome in Madelung's deformity.
    Luchetti R, Mingione A, Monteleone M, Cristiani G.
    J Hand Surg Br; 1988 Feb; 13(1):19-22. PubMed ID: 3361201
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  • 24. [Leri-Weill dyschondrosteosis].
    Fernández Mariño EA, de Oya Pardo G.
    Rev Clin Esp; 1981 Sep 15; 162(5):235-7. PubMed ID: 6975956
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  • 26. 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 15; 170A(4):949-57. PubMed ID: 26698168
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  • 29. Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Léri-Weill dyschondrosteosis, developmental delay, and ichthyosis.
    Vassal H, Medeira A, Cordeiro I, Santos HG, Castedo S, Saraiva C, da Silva PM, Monteiro C.
    Am J Med Genet; 2001 Apr 01; 99(4):331-4. PubMed ID: 11252003
    [No Abstract] [Full Text] [Related]

  • 30. Madelung's deformity: a spectrum of presentation.
    Zebala LP, Manske PR, Goldfarb CA.
    J Hand Surg Am; 2007 Nov 01; 32(9):1393-401. PubMed ID: 17996774
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  • 35. Acrodysostosis in two generations: an autosomal dominant syndrome.
    Hernández RM, Miranda A, Kofman-Alfaro S.
    Clin Genet; 1991 May 01; 39(5):376-82. PubMed ID: 1860254
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  • 36. Madelung's deformity: quantitative radiographic comparison with normal wrists.
    McCarroll HR, James MA, Newmeyer WL, Manske PR.
    J Hand Surg Eur Vol; 2008 Oct 01; 33(5):632-5. PubMed ID: 18694918
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  • 38. Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: report of a pedigree with autosomal dominant inheritance.
    MacDermot KD, Roth SC, Hall C, Winter RM.
    J Med Genet; 1987 Oct 01; 24(10):602-8. PubMed ID: 3681905
    [Abstract] [Full Text] [Related]

  • 39. Brachydactyly type A1 with short humerus and associated skeletal features.
    Lacombe D, Delrue MA, Rooryck C, Morice-Picard F, Arveiler B, Maugey-Laulom B, Mundlos S, Toutain A, Chateil JF.
    Am J Med Genet A; 2010 Dec 01; 152A(12):3016-21. PubMed ID: 21077205
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  • 40. Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male.
    Stuppia L, Calabrese G, Borrelli P, Gatta V, Morizio E, Mingarelli R, Di Gilio MC, Crinò A, Giannotti A, Rappold GA, Palka G.
    J Med Genet; 1999 Sep 01; 36(9):711-3. PubMed ID: 10507731
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