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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

133 related items for PubMed ID: 12833413

  • 41. Metaphyseal anadysplasia in two sisters.
    Slama M, Mathieu M, Dehouck I, al Hosri J, Vanthournout I, Baratte B, Grumbach Y.
    Pediatr Radiol; 1999 May; 29(5):372-5. PubMed ID: 10382218
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  • 42. Bilateral hereditary micro-epiphyseal dysplasia: further delineation of the phenotype with 40 years follow-up.
    Mostert AK, Jansen BR, Dijkstra PF, Wesby-van Swaay E, van Horn JR, Heutink P, Lindhout D.
    Int Orthop; 2002 May; 26(3):188-93. PubMed ID: 12073115
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  • 44. Spondyloenchondrodysplasia: a rare cause of short stature.
    Yeşiltepe-Mutlu G, Ozsu E, Cizmecioğlu FM, Alanay Y, Hatun S.
    Turk J Pediatr; 2011 May; 53(4):464-6. PubMed ID: 21980854
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  • 45. Spondyloenchondrodysplasia. Enchondromatomosis with severe platyspondyly in two brothers.
    Schorr S, Legum C, Ochshorn M.
    Radiology; 1976 Jan; 118(1):133-9. PubMed ID: 1244645
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  • 48. Further evidence of POP1 mutations as the cause of anauxetic dysplasia.
    Elalaoui SC, Laarabi FZ, Mansouri M, Mrani NA, Nishimura G, Sefiani A.
    Am J Med Genet A; 2016 Sep; 170(9):2462-5. PubMed ID: 27380734
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  • 49. A new form of severe spondyloepimetaphyseal dysplasia: clinical and radiological characterization.
    Isidor B, Geffroy L, de Courtivron B, Le Caignec C, Thiel CT, Mortier G, Cormier-Daire V, David A, Toutain A.
    Am J Med Genet A; 2013 Oct; 161A(10):2645-51. PubMed ID: 23956136
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  • 50. A case with spondylo-metaphyseal dysplasia type A4.
    Percin EF, Tukenmez M, Percin S.
    Genet Couns; 2004 Oct; 15(3):363-9. PubMed ID: 15517830
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  • 52. Congenital hypothyroidism presenting as apparent spondyloepiphyseal dysplasia.
    Eberle AJ.
    Am J Med Genet; 1993 Sep 15; 47(4):464-7. PubMed ID: 8256805
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  • 54. [Spondylo-epiphyseal dysplasia. Description of a family].
    Bonora G, Manzoni D, Rogari P, Pizzi E, Andreoli A, Nedbal M.
    Pediatr Med Chir; 1988 Sep 15; 10(1):111-4. PubMed ID: 3375124
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  • 57. Further delineation of spondyloepimetaphyseal dysplasia Faden-Alkuraya type: A RSPRY1-associated spondylo-epi-metaphyseal dysplasia with cono-brachydactyly and craniosynostosis.
    Simsek-Kiper PO, Taskiran EZ, Kosukcu C, Urel-Demir G, Akgun-Dogan O, Yilmaz G, Utine GE, Nishimura G, Boduroglu K, Alikasifoglu M.
    Am J Med Genet A; 2018 Sep 15; 176(9):2009-2016. PubMed ID: 30063090
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  • 58. Pseudoachondroplastic dysplasia.
    Khungar A, Mahajan P, Gupte G, Vasundhara M, Kher A, Bharucha BA.
    J Postgrad Med; 1993 Sep 15; 39(2):91-3. PubMed ID: 8169872
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