A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type ia (PHP Ia) and normal calcium and phosphate levels (2010)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: MUTAÇÃO GENÉTICA; OBESIDADE (GENÉTICA); FENÓTIPOS; DOENÇAS GENÉTICAS; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP"
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ABNT
REIS, M T A et al. A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type ia (PHP Ia) and normal calcium and phosphate levels. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 2010 -
APA
Reis, M. T. A., Cattani, A., Castillo, C., Mendonça, B. B. de, Correa, P. H. S., & Martin, R. M. (2010). A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type ia (PHP Ia) and normal calcium and phosphate levels. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Reis MTA, Cattani A, Castillo C, Mendonça BB de, Correa PHS, Martin RM. A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type ia (PHP Ia) and normal calcium and phosphate levels. Clinics. 2010 ; 65 S73.[citado 2024 abr. 19 ] -
Vancouver
Reis MTA, Cattani A, Castillo C, Mendonça BB de, Correa PHS, Martin RM. A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type ia (PHP Ia) and normal calcium and phosphate levels. Clinics. 2010 ; 65 S73.[citado 2024 abr. 19 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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