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Journal Abstract Search


158 related items for PubMed ID: 1244645

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  • 4. Dysmorphic facies and diffuse posterior spine ankylosis in a patient with unusual form of spondyloenchondrodysplasia (Spranger type IV).
    Al Kaissi A, Ben Chehida F, Ben Ghachem M, Klaushofer K, Grill F.
    Eur Spine J; 2013 May; 22 Suppl 3(Suppl 3):S409-15. PubMed ID: 23053755
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  • 5. Spondyloenchondrodysplasia: clinical variability in three cases.
    Tüysüz B, Arapoglu M, Ungür S.
    Am J Med Genet A; 2004 Jul 15; 128A(2):185-9. PubMed ID: 15214014
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  • 7. Short trunk stature, brachydactyly, and platyspondyly in three sibs: a new form of brachyolmia or a new skeletal dysplasia?
    Tüysüz B, Ungür S.
    Am J Med Genet A; 2003 Jun 15; 119A(3):375-80. PubMed ID: 12784309
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  • 8. Autosomal dominant inheritance of spondyloenchondrodysplasia.
    Bhargava R, Leonard NJ, Chan AK, Spranger J.
    Am J Med Genet A; 2005 Jun 15; 135(3):282-8. PubMed ID: 15887273
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  • 10. Case report 418: Multiple enchondromatosis (Ollier disease) with severe vertebral changes.
    Azouz EM.
    Skeletal Radiol; 1987 Jun 15; 16(3):236-9. PubMed ID: 3589742
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  • 12. [Late spondyloepiphysial dysplasia].
    DUBOST J, DUBOST E, PICARD JM.
    J Radiol Electrol Med Nucl; 1961 Jun 15; 42():386-9. PubMed ID: 13724643
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  • 19. [Hereditary chondrodysplasias].
    Piffaretti PG.
    Radiol Clin Biol; 1969 Jun 15; 38(2):97-114. PubMed ID: 4240528
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  • 20. Monogenic lupus due to spondyloenchondrodysplasia with spastic paraparesis and intracranial calcification: case-based review.
    Kara B, Ekinci Z, Sahin S, Gungor M, Gunes AS, Ozturk K, Adrovic A, Cefle A, Inanç M, Gul A, Kasapcopur O.
    Rheumatol Int; 2020 Nov 15; 40(11):1903-1910. PubMed ID: 32691099
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