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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

119 related items for PubMed ID: 12069472

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  • 4. A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia.
    Tsai FJ, Wu JY, Lin WD, Tsai CH.
    Acta Paediatr; 2000 Oct; 89(10):1262-5. PubMed ID: 11083386
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  • 5. [Cleidocranial dysostosis (Pierre-Marie and Santon's disease)].
    Popović V, Popović S, Nedić LJ.
    Acta Chir Iugosl; 1975 Oct; 22(1 Suppl):123-6. PubMed ID: 1235604
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  • 10. [3 cases of cleidocranial dysostosis].
    Zamperoni A, Andreoni A, Grasso G.
    Chir Organi Mov; 1989 Oct; 74(3-4):127-35. PubMed ID: 2635654
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  • 14. [Etiopathogenesis of cleidocranial dysostosis].
    De Giorgi G.
    Chir Organi Mov; 1971 Oct; 60(2):97-103. PubMed ID: 5162984
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  • 15. [A case of cleidocranial dysostosis].
    Herzog B, Delobel R, Albert M.
    J Radiol Electrol Med Nucl; 1970 Dec; 51(12):809-11. PubMed ID: 5510218
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  • 16. Cleidocranial dysplasia: radiological appearances on dental panoramic radiography.
    McNamara CM, O'Riordan BC, Blake M, Sandy JR.
    Dentomaxillofac Radiol; 1999 Mar; 28(2):89-97. PubMed ID: 10522197
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  • 19. RUNX genes, neoplasia, and cleidocranial dysplasia.
    Cohen MM.
    Am J Med Genet; 2001 Dec 01; 104(3):185-8. PubMed ID: 11754042
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  • 20. Cleidocranial dysplasia associated with a t(6;18)(p12;q24) translocation.
    Narahara K, Tsuji K, Yokoyama Y, Seino Y.
    Am J Med Genet; 1995 Mar 13; 56(1):119-20. PubMed ID: 7747775
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