Search Results - Maryam Alsada

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    Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His by Mohamed Aashiq, Asma Jassim Malallah, Farheen Khan, Maryam Alsada

    Published 2020
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