bibliographic entry 12697271 [be/12697271]
https://w3id.org/oc/corpus/be/12697271
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Kasahara, T, Narumi, S, Okasora, K. Delayed onset congenital hypothyroidism in a patient with DUOX2 mutations and maternal iodine excess, Am. J. Med. Genet. A, 161A, 2013, 214, 217, PMID: 23239635
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