Hasil Pencarian - Addison Mark K

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    Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: Relevance to ocular dysgenesis and hearing impairment

    Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: Relevance to ocular dysgenesis and hearing impairment oleh Ritch Robert, Munier Francis, Addison Mark K, Jaafar Mohamad S, Gould Douglas B, MacDonald Ian M, Walter Michael A

    Diterbitkan 2004-06-01
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