Absence of inactivating mutations in FGF9 and FGFR2, genes 46,XY patients with disorders of sex development (DSD) due to gonodal dysgenesis (2010)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: MUTAÇÃO GENÉTICA; TRANSTORNOS GONADAIS; 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
MACHADO, A Z et al. Absence of inactivating mutations in FGF9 and FGFR2, genes 46,XY patients with disorders of sex development (DSD) due to gonodal dysgenesis. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 2010 -
APA
Machado, A. Z., Santos, M. G., Costa, E. M. F., Mendonça, B. B. de, Gomes, C. R., Brandão, M. P., et al. (2010). Absence of inactivating mutations in FGF9 and FGFR2, genes 46,XY patients with disorders of sex development (DSD) due to gonodal dysgenesis. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Machado AZ, Santos MG, Costa EMF, Mendonça BB de, Gomes CR, Brandão MP, Nishi MY, Silva RB, Domenice S. Absence of inactivating mutations in FGF9 and FGFR2, genes 46,XY patients with disorders of sex development (DSD) due to gonodal dysgenesis. Clinics. 2010 ; 65 S66.[citado 2024 abr. 24 ] -
Vancouver
Machado AZ, Santos MG, Costa EMF, Mendonça BB de, Gomes CR, Brandão MP, Nishi MY, Silva RB, Domenice S. Absence of inactivating mutations in FGF9 and FGFR2, genes 46,XY patients with disorders of sex development (DSD) due to gonodal dysgenesis. Clinics. 2010 ; 65 S66.[citado 2024 abr. 24 ] - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
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