Borges, M. d. F. (2019). A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING. Sociedade de Pediatria de São Paulo.
Citazione stile Chigago Style (17a edizione)Borges, Maria de Fátima. A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING. Sociedade de Pediatria de São Paulo, 2019.
Citatione MLA (9a ed.)Borges, Maria de Fátima. A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING. Sociedade de Pediatria de São Paulo, 2019.
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