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    Congenital hypothyroidism as the initial presentation of pendred syndrome associated with mutated IVS7-2A>G in SLC26A4 gene in a Taiwanese neonate

    Congenital hypothyroidism as the initial presentation of pendred syndrome associated with mutated IVS7-2A>G in SLC26A4 gene in a Taiwanese neonate by Sun-Mei Chung, Yu-Wen Pan, Yi-Shan Tsai, Meng-Che Tsai

    Published 2023-01-01
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