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Journal Abstract Search

186 related items for PubMed ID: 16206059

  • 1. Dyggve-Melchior-Clausen syndrome without mental retardation (Smith-McCort dysplasia).
    Bayrak IK, Nural MS, Diren HB.
    Diagn Interv Radiol; 2005 Sep; 11(3):163-5. PubMed ID: 16206059
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  • 3. Dyggve melchior clausen syndrome.
    Gupta V, Kohli A, Dewan V.
    Indian Pediatr; 2010 Nov; 47(11):973-5. PubMed ID: 21149903
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  • 4. The Dyggve-Melchio-Clausen syndrome.
    Schorr S, Legum C, Ochshorn M, Hirsch M, Moses S, Lasch EE, El-Masri M.
    AJR Am J Roentgenol; 1977 Jan; 128(1):107-13. PubMed ID: 401564
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  • 7. Bilateral Severe Genu Varum in Dyggve-Melchior-Clausen Syndrome - A Case Report.
    Yadav AK, Wadia F, Gawhale S, Panchal S, Talukder P, Mokashi M.
    J Orthop Case Rep; 2021 Aug; 11(8):84-86. PubMed ID: 35004383
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  • 8. [Smith-McCort syndrome (author's transl)].
    Koppers B.
    Rofo; 1979 Feb; 130(2):213-22. PubMed ID: 154455
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  • 9. Dyggve-Melchior-Clausen syndrome: report of seven patients with the Smith-McCort variant and review of the literature.
    Burns C, Powell BR, Hsia YE, Reinker K.
    J Pediatr Orthop; 2003 Feb; 23(1):88-93. PubMed ID: 12499951
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  • 11. Evidence that Smith-McCort dysplasia and Dyggve-Melchior-Clausen dysplasia are allelic disorders that result from mutations in a gene on chromosome 18q12.
    Ehtesham N, Cantor RM, King LM, Reinker K, Powell BR, Shanske A, Unger S, Rimoin DL, Cohn DH.
    Am J Hum Genet; 2002 Oct; 71(4):947-51. PubMed ID: 12161821
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  • 13. [Dyggve-Melchior-Clausen syndrome, diagnostic difficulty due to it similarity to Morquio disease].
    Rodríguez Rodríguez CM, Pineda Marfa M, Duque R, Cormier-Daire V.
    Neurologia; 2007 Mar; 22(2):126-9. PubMed ID: 17323241
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  • 17. The Dyggve-Melchior-Clausen syndrome.
    Spranger J, Maroteaux P, Der Kaloustian VM.
    Radiology; 1975 Feb; 114(2):415-21. PubMed ID: 803318
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  • 18. Dyggve-Melchior-Clausen syndrome: genetic studies and report of affected sibs.
    Toledo SP, Saldanha PH, Lamego C, Mourão PA, Dietrich CP, Mattar E.
    Am J Med Genet; 1979 Feb; 4(3):255-61. PubMed ID: 117710
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  • 19. A novel RAB33B mutation in Smith-McCort dysplasia.
    Dupuis N, Lebon S, Kumar M, Drunat S, Graul-Neumann LM, Gressens P, El Ghouzzi V.
    Hum Mutat; 2013 Feb; 34(2):283-6. PubMed ID: 23042644
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  • 20. Probable identity-by-descent for a mutation in the Dyggve-Melchior-Clausen/Smith-McCort dysplasia (Dymeclin) gene among patients from Guam, Chile, Argentina, and Spain.
    Pogue R, Ehtesham N, Repetto GM, Carrero-Valenzuela R, de Casella CB, de Pons SP, Martínez-Frías ML, Heuertz S, Cormier-Daire V, Cohn DH.
    Am J Med Genet A; 2005 Sep 15; 138(1):75-8. PubMed ID: 16097008
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