Source: The Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Subjects: HIPOTIREOIDISMO, MÃES, CRIANÇAS
ABNT
CONGDON, Tamara et al. A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child. The Journal of Clinical Endocrinology & Metabolism, v. 8, n. 86, p. 3962-3967, 2001Tradução . . Acesso em: 18 out. 2024.APA
Congdon, T., Nguyen, L. Q., Nogueira, C. R., Habiby, R. L., Kopp, P., & Medeiros Neto, G. (2001). A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child. The Journal of Clinical Endocrinology & Metabolism, 8( 86), 3962-3967.NLM
Congdon T, Nguyen LQ, Nogueira CR, Habiby RL, Kopp P, Medeiros Neto G. A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child. The Journal of Clinical Endocrinology & Metabolism. 2001 ; 8( 86): 3962-3967.[citado 2024 out. 18 ]Vancouver
Congdon T, Nguyen LQ, Nogueira CR, Habiby RL, Kopp P, Medeiros Neto G. A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child. The Journal of Clinical Endocrinology & Metabolism. 2001 ; 8( 86): 3962-3967.[citado 2024 out. 18 ]