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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

159 related items for PubMed ID: 24954533

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  • 9. One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.
    Afzal AR, Jeffery S.
    Hum Mutat; 2003 Jul; 22(1):1-11. PubMed ID: 12815588
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  • 11. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.
    Afzal AR, Rajab A, Fenske CD, Oldridge M, Elanko N, Ternes-Pereira E, Tüysüz B, Murday VA, Patton MA, Wilkie AO, Jeffery S.
    Nat Genet; 2000 Aug; 25(4):419-22. PubMed ID: 10932186
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  • 13. 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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  • 14. 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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