Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations

Pardo‚ V.; Rubio‚ I.G.S.; Knobel‚ M.; Aguiar-Oliveira‚ M.H.; Santos‚ M.M.; Gomes‚ S.A.; Oliveira‚ C.R.P.; Targovnik‚ H.M.; Medeiros-Neto‚ G.

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(Reference retrieved automatically from Google Scholar through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations

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Author(s):	Pardo‚ V. ; Rubio‚ I.G.S. ; Knobel‚ M. ; Aguiar-Oliveira‚ M.H. ; Santos‚ M.M. ; Gomes‚ S.A. ; Oliveira‚ C.R.P. ; Targovnik‚ H.M. ; Medeiros-Neto‚ G. Total Authors: 9
Document type:	Journal article
Source:	THYROID; v. 18, n. 7, p. 783-786, 2008.

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