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    Clin Genet. 2012 Mar;81(3):294-7. doi: 10.1111/j.1399-0004.2011.01730.x. Epub 2011 Dec 28.

    PRRX1 is mutated in an otocephalic newborn infant conceived by consanguineous parents.

    PMID:
    22211708
    [PubMed - in process]

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