Molecular study of SRY gene in patients with 45,X gonadal dysgenesis and its variants (2007)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: BIOLOGIA MOLECULAR; TRANSTORNOS GONADAIS; MUTAÇÃO GENÉTICA; RESUMOS (SIMPÓSIOS)
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Simpósio avanços em pesquisas médicas
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ABNT
NISHI, M. Y. et al. Molecular study of SRY gene in patients with 45,X gonadal dysgenesis and its variants. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 16 out. 2024. , 2007 -
APA
Nishi, M. Y., Medeiros, M. E., Costa, E. M. F., Oliveira, S. B., Brenlha, I. N., Ueti, R. C., et al. (2007). Molecular study of SRY gene in patients with 45,X gonadal dysgenesis and its variants. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Nishi MY, Medeiros ME, Costa EMF, Oliveira SB, Brenlha IN, Ueti RC, Mendonça BB de, Domenice S. Molecular study of SRY gene in patients with 45,X gonadal dysgenesis and its variants. Clinics. 2007 ; 62 S86.[citado 2024 out. 16 ] -
Vancouver
Nishi MY, Medeiros ME, Costa EMF, Oliveira SB, Brenlha IN, Ueti RC, Mendonça BB de, Domenice S. Molecular study of SRY gene in patients with 45,X gonadal dysgenesis and its variants. Clinics. 2007 ; 62 S86.[citado 2024 out. 16 ] - Reavaliação na idade adulta do diagnóstico da deficiência de GH (DGH) determinado na infância
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