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A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation.
Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1337-44. doi: 10.1590/s0004-27302008000800022.
Arq Bras Endocrinol Metabol. 2008.
PMID: 19169491
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