Search Results - Ammouri, Farah

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    P724: A unique presentation of triple X syndrome with four copies of SHOX and additional low-level aneuploidy mosaicism

    P724: A unique presentation of triple X syndrome with four copies of SHOX and additional low-level aneuploidy mosaicism by Spaulding, Joanna, Ammouri, Farah, Nielsen, Shelly, VanDyke, Zephyr, Koerselman, Haley, Zaleski, Dianna, Althof, Pamela, Lulla, Dinesh

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    Pancreatitis is an FGF21-deficient state that is corrected by replacement therapy

    Pancreatitis is an FGF21-deficient state that is corrected by replacement therapy by Hernandez, Genaro, Luo, Ting, Javed, Tanveer A, Wen, Li, Kalwat, Michael A, Vale, Kevin, Ammouri, Farah, Husain, Sohail Z, Kliewer, Steven A, Mangelsdorf, David J

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