A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child (2001)
- Authors:
- Autor USP: MEDEIROS NETO, GERALDO ANTONIO DE - FM
- Unidade: FM
- Subjects: HIPOTIREOIDISMO; MÃES; CRIANÇAS
- Language: Inglês
- Imprenta:
- Source:
- Título: The Journal of Clinical Endocrinology & Metabolism
- Volume/Número/Paginação/Ano: v. 8, n. 86, p. 3962-3967, ago. 2001
-
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: 07 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. 07 ] -
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. 07 ] - Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect
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