Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ von Ebrhim, Reham S., Bruellman, Ryan J., Watanabe, Yui, Creech, Matthew K., Abdullah, Mohamed A., Dumitrescu, Alexandra M., Refetoff, Samuel, Weiss, Roy E.

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Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism von Bruellman, Ryan J, Watanabe, Yui, Ebrhim, Reham S, Creech, Matthew K, Abdullah, Mohamed A, Dumitrescu, Alexandra M, Refetoff, Samuel, Weiss, Roy E

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A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism von Watanabe, Yui, Ebrhim, Reham S., Abdullah, Mohamed A., Weiss, Roy E.

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Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families von Watanabe, Yui, Bruellman, Ryan J., Ebrhim, Reham S., Abdullah, Mohamed A., Dumitrescu, Alexandra M., Refetoff, Samuel, Weiss, Roy E.

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Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ von Ebrhim, Reham S, Bruellman, Ryan J, Watanabe, Yui, Creech, Matthew K, Abdullah, Mohamed A, Dumitrescu, Alexandra M, Refetoff, Samuel, Weiss, Roy E

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