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G D Frechtel

Showing results (1-10 of 4) with videos related to

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Thyroid : Official Journal of the American Thyroid Association|May 20, 1998
Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a Brazilian family with congenital goiter and hypothyroidismH M Targovnik, G D Frechtel, F M Mendive, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|December 1, 1994
Molecular genetics of hereditary thyroid diseases due to a defect in the thyroglobulin or thyroperoxidase synthesisH M Targovnik, V Varela, G D Frechtel, et al.
Journal of Endocrinological Investigation|June 1, 1993
Human thyroid tissue do not express thyroalbuminH M Targovnik, G D Frechtel, V Varela, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 10, 2009
Glucokinase gene mutation screening in Argentinean clinically characterized MODY patientsA P Lopez, S A Foscaldi, M S Pérez, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Thyroid : Official Journal of the American Thyroid Association|May 20, 1998
Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a Brazilian family with congenital goiter and hypothyroidismH M Targovnik, G D Frechtel, F M Mendive, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|December 1, 1994
Molecular genetics of hereditary thyroid diseases due to a defect in the thyroglobulin or thyroperoxidase synthesisH M Targovnik, V Varela, G D Frechtel, et al.
Journal of Endocrinological Investigation|June 1, 1993
Human thyroid tissue do not express thyroalbuminH M Targovnik, G D Frechtel, V Varela, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 10, 2009
Glucokinase gene mutation screening in Argentinean clinically characterized MODY patientsA P Lopez, S A Foscaldi, M S Pérez, et al.
Pageof 1