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Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|July 15, 2004
The syndrome of resistance to thyroid hormone, misdiagnosed and treated as thyrotoxicosisI A Mohammed, S Aldasouqi, R Schnute, et al.
Human Genetics|April 1, 1989
Eco RI RFLP in the human thyroid peroxidase (TPO) gene on chromosome 2H Bikker, P A Bolhuis, G Vassart, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1993
A nonsense mutation causes human hereditary congenital goiter with preferential production of a 171-nucleotide-deleted thyroglobulin ribonucleic acid messengerH M Targovnik, G Medeiros-Neto, V Varela, et al.
Cellular and Molecular Life Sciences : CMLS|April 29, 2008
The specificity of binding of glycoprotein hormones to their receptorsG Caltabiano, M Campillo, A De Leener, et al.
Thyroid : Official Journal of the American Thyroid Association|January 26, 2000
Improved radioimmunoassay for measurement of mouse thyrotropin in serum: strain differences in thyrotropin concentration and thyrotroph sensitivity to thyroid hormoneJ Pohlenz, A Maqueem, K Cua, et al.
Clinical Endocrinology|January 1, 1977
Familial goitre with partial iodine organification defect, lack of thyroglobulin, and high levels of thyroid peroxidaseH Niepomniszcze, G A Medeiros-Neto, S Refetoff, et al.
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