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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

111 related items for PubMed ID: 6496568

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  • 10. [Autosomal recessive metaphyseal chondrodysplasia and Hirschsprung's disease].
    le Merrer M, Briard ML, Chauvet ML, Maroteaux P.
    Ann Pediatr (Paris); 1991 Jan; 38(1):27-30. PubMed ID: 2006830
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  • 14. Enchondromatosis with features of dysspondyloenchondromatosis and Maffucci syndrome.
    Haga N, Nakamura K, Taniguchi K, Nakamura S.
    Clin Dysmorphol; 1998 Jan; 7(1):65-8. PubMed ID: 9546836
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  • 16. [Neuropathological findings in a case of fetal chondrodysplasia].
    Galatioto S, Nicotina PA, Deodato M.
    Arch De Vecchi Anat Patol; 1980 Jan; 64(1):103-5. PubMed ID: 7294855
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  • 17. Atypical chondrodysplasia: a further variant of multiple enchondromatosis with vertebral involvement?
    Hegarty SE, Fairhurst JJ, Temple IK.
    Pediatr Radiol; 1998 Dec; 28(12):963-6. PubMed ID: 9880642
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  • 18. Spondylometaphyseal dysplasia, east-African type: a new form of early, severe SMD with rounded vertebrae.
    Verloes A, Lepage P, Baumann C, Maroteaux P, Merrer ML.
    Am J Med Genet; 2002 Dec 15; 113(4):362-6. PubMed ID: 12457408
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  • 20. Possible heterogeneity in spondyloenchondrodysplasia: quadriparesis, basal ganglia calcifications, and chondrocyte inclusions.
    Frydman M, Bar-Ziv J, Preminger-Shapiro R, Brezner A, Brand N, Ben-Ami T, Lachman RS, Gruber HE, Rimoin DL.
    Am J Med Genet; 1990 Jul 15; 36(3):279-84. PubMed ID: 2363422
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