Genetic linkage studies of thyroid peroxidase (tpo) gene in families with tpo deficiency (1991)
- Authors:
- USP affiliated authors: WAJCHENBERG, BERNARDO LEO - FM ; MEDEIROS NETO, GERALDO ANTONIO DE - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Source:
- Título: Journal of Clinical Endocrinology and Metabolism
- Volume/Número/Paginação/Ano: v.72, n.2 , p.471-6, feb. 1991
- Conference titles: International Symposium on Thyroperoxidase and Thyroid Autoimmunity
-
ABNT
MANGKLABRUKS, A et al. Genetic linkage studies of thyroid peroxidase (tpo) gene in families with tpo deficiency. Journal of Clinical Endocrinology and Metabolism. [S.l.]: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 17 out. 2024. , 1991 -
APA
Mangklabruks, A., Billerbeck, A. E. C., Wajchenberg, B. L., Knobel, M., Cox, N. J., De Groot, L. J., & Medeiros Neto, G. A. (1991). Genetic linkage studies of thyroid peroxidase (tpo) gene in families with tpo deficiency. Journal of Clinical Endocrinology and Metabolism. Faculdade de Medicina, Universidade de São Paulo. -
NLM
Mangklabruks A, Billerbeck AEC, Wajchenberg BL, Knobel M, Cox NJ, De Groot LJ, Medeiros Neto GA. Genetic linkage studies of thyroid peroxidase (tpo) gene in families with tpo deficiency. Journal of Clinical Endocrinology and Metabolism. 1991 ;72( 2 ): 471-6.[citado 2024 out. 17 ] -
Vancouver
Mangklabruks A, Billerbeck AEC, Wajchenberg BL, Knobel M, Cox NJ, De Groot LJ, Medeiros Neto GA. Genetic linkage studies of thyroid peroxidase (tpo) gene in families with tpo deficiency. Journal of Clinical Endocrinology and Metabolism. 1991 ;72( 2 ): 471-6.[citado 2024 out. 17 ] - 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 defective thyroglobulin synthesis
- Human thyroid tissue do not express thyroalbumin
- 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 goiter with defective thyroglobulin
- Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism
- Defective organification of iodice causing hereditary goitrous hypothyroidism
- Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
