Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism (1993)
- Authors:
- USP affiliated authors: WAJCHENBERG, BERNARDO LEO - FM ; MEDEIROS NETO, GERALDO ANTONIO DE - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Progress in Endocrinology
- Conference titles: International Congress of the Endocrinology
-
ABNT
MEDEIROS NETO, Geraldo Antônio e BILLERBECK, A E C e WAJCHENBERG, B L. Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. 1993, Anais.. Carnforth: Parthenon, 1993. . Acesso em: 19 abr. 2024. -
APA
Medeiros Neto, G. A., Billerbeck, A. E. C., & Wajchenberg, B. L. (1993). Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. In Progress in Endocrinology. Carnforth: Parthenon. -
NLM
Medeiros Neto GA, Billerbeck AEC, Wajchenberg BL. Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. Progress in Endocrinology. 1993 ;[citado 2024 abr. 19 ] -
Vancouver
Medeiros Neto GA, Billerbeck AEC, Wajchenberg BL. Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. Progress in Endocrinology. 1993 ;[citado 2024 abr. 19 ] - Effect of hypocaloric diet with and without d-fenfluramine treatment on growth hormone release after growth hormone-releasing factor stimulation in patients with android obesity
- Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin
- Hyposialylated thyroglobulin in a patient with congenital goiter and hypothyroidism
- 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis
- Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger
- Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis
- Human thyroid tissue do not express thyroalbumin
- Genetic linkage studies of thyroid peroxidase (tpo) gene in families with tpo deficiency
- Defective organification of iodice causing hereditary goitrous hypothyroidism
- Thyroid peroxidase (tpo) gene polymorphisms in subjets with prended's syndrome
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