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Delayed onset congenital hypothyroidism in a patient with DUOX2 mutations and maternal iodine excess

✍ Scribed by Kasahara, Toshihiko; Narumi, Satoshi; Okasora, Keisuke; Takaya, Ryuzo; Tamai, Hiroshi; Hasegawa, Tomonobu


Book ID
118751183
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
146 KB
Volume
161
Category
Article
ISSN
1552-4825

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