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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

177 related items for PubMed ID: 19236432

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  • 5. Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome.
    van Bokhoven H, Celli J, Kayserili H, van Beusekom E, Balci S, Brussel W, Skovby F, Kerr B, Percin EF, Akarsu N, Brunner HG.
    Nat Genet; 2000 Aug; 25(4):423-6. PubMed ID: 10932187
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  • 10. WNT5A mutations in patients with autosomal dominant Robinow syndrome.
    Person AD, Beiraghi S, Sieben CM, Hermanson S, Neumann AN, Robu ME, Schleiffarth JR, Billington CJ, van Bokhoven H, Hoogeboom JM, Mazzeu JF, Petryk A, Schimmenti LA, Brunner HG, Ekker SC, Lohr JL.
    Dev Dyn; 2010 Jan; 239(1):327-37. PubMed ID: 19918918
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  • 11. Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.
    Oldridge M, Fortuna AM, Maringa M, Propping P, Mansour S, Pollitt C, DeChiara TM, Kimble RB, Valenzuela DM, Yancopoulos GD, Wilkie AO.
    Nat Genet; 2000 Mar; 24(3):275-8. PubMed ID: 10700182
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  • 13. Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B.
    Wang B, Sinha T, Jiao K, Serra R, Wang J.
    Hum Mol Genet; 2011 Jan 15; 20(2):271-85. PubMed ID: 20962035
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  • 14. Clinical and molecular characterization of two adults with autosomal recessive Robinow syndrome.
    Tufan F, Cefle K, Türkmen S, Türkmen A, Zorba U, Dursun M, Oztürk S, Palandüz S, Ecder T, Mundlos S, Horn D.
    Am J Med Genet A; 2005 Jul 15; 136(2):185-9. PubMed ID: 15952209
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