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Pubmed for Handhelds

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Journal Abstract Search

165 related items for PubMed ID: 9324546

  • 21. [Bilateral cataract in childhood years: always an indication for screening on a metabolic disorder].
    Wijburg MT, Wenniger-Prick LJ, Bosch AM, Visser G, Bams-Mengerink A.
    Ned Tijdschr Geneeskd; 2008 Mar 15; 152(11):632-6. PubMed ID: 18410025
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  • 23. Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations.
    Akawi NA, Al-Gazali L, Ali BR.
    Clin Genet; 2012 Aug 15; 82(2):147-56. PubMed ID: 21668896
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  • 28. Evidence of postzygotic mosaicism in a transmitted form of Conradi-Hunermann-Happle syndrome associated with a novel EBP mutation.
    Morice-Picard F, Kostrzewa E, Wolf C, Benlian P, Taïeb A, Lacombe D.
    Arch Dermatol; 2011 Sep 15; 147(9):1073-6. PubMed ID: 21931045
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  • 34. Hypertelorism-microtia-clefting (HMC) syndrome.
    Verloes A.
    Genet Couns; 1994 Sep 15; 5(3):283-7. PubMed ID: 7811429
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