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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

129 related items for PubMed ID: 20677139

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  • 2. Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family.
    Liu M, Ke T, Wang Z, Yang Q, Chang W, Jiang F, Tang Z, Li H, Ren X, Wang X, Wang T, Li Q, Yang J, Liu J, Wang QK.
    Invest Ophthalmol Vis Sci; 2006 Aug; 47(8):3461-6. PubMed ID: 16877416
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  • 8. Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedema.
    Gordon K, Schulte D, Brice G, Simpson MA, Roukens MG, van Impel A, Connell F, Kalidas K, Jeffery S, Mortimer PS, Mansour S, Schulte-Merker S, Ostergaard P.
    Circ Res; 2013 Mar 15; 112(6):956-60. PubMed ID: 23410910
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  • 12. A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataract.
    Ding X, Zhou N, Lin H, Chen J, Zhao C, Zhou G, Hejtmancik JF, Qi Y.
    PLoS One; 2014 Mar 15; 9(7):e102733. PubMed ID: 25033405
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