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Autor:
C L, Santos, H, Bikker, K G, Rego, A C, Nascimento, M, Tambascia, J J, De Vijlder, G, Medeiros-Neto
Publikováno v:
Clinical endocrinology. 51(2)
To screen and subsequently sequence the TPO gene for mutations in patients with congenital goitre, hypothyroidism and evidence for an organification defect (positive perchlorate discharge test).We have studied seven hypothyroid and congenitally goitr