Recurrence of the p.R277X/p.R1511X compound heterozygous mutation in the thyroglobulin gene in unrelated families with congenital goiter and hypothyroidism: Haplotype analysis using intragenic thyroglobulin polymorphisms

1. Caputo, M.
2. Rivolta, C.M.
3. Gutnisky, V.J.
4. Gruñeiro-Papendieck, L.
5. Chiesa, A.
6. Medeiros-Neto, G.
7. González-Sarmiento, R.
8. Targovnik, H.M.

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DOI: 10.1677/JOE-07-0033 GOOGLE SCHOLAR lock_openOpen access editor

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