A novel missense variant in the Necdin gene in a male patient with kallmann syndrome (2010)
- Autores:
- Autores USP: MENDONÇA, BERENICE BILHARINHO DE - FM ; XAVIER, ANA CLAUDIA LATRÔNICO - FM
- Unidade: FM
- Assuntos: HIPOGONADISMO (GENÉTICA); SÍNDROME DE KALLMANN (CONGÊNITO;GENÉTICA); MAPEAMENTO CROMOSSÔMICO; RESUMOS (EVENTOS)
- Idioma: Inglês
- Imprenta:
- Fonte:
- Nome do evento: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP"
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ABNT
BENEDUZZI, D et al. A novel missense variant in the Necdin gene in a male patient with kallmann syndrome. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 26 abr. 2024. , 2010 -
APA
Beneduzzi, D., Silveira-Neto, A. P., Trarbach, E., Mendonça, B. B. de, Xavier, A. C. L., & Fragoso, M. C. B. V. (2010). A novel missense variant in the Necdin gene in a male patient with kallmann syndrome. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Beneduzzi D, Silveira-Neto AP, Trarbach E, Mendonça BB de, Xavier ACL, Fragoso MCBV. A novel missense variant in the Necdin gene in a male patient with kallmann syndrome. Clinics. 2010 ; 65 S62.[citado 2024 abr. 26 ] -
Vancouver
Beneduzzi D, Silveira-Neto AP, Trarbach E, Mendonça BB de, Xavier ACL, Fragoso MCBV. A novel missense variant in the Necdin gene in a male patient with kallmann syndrome. Clinics. 2010 ; 65 S62.[citado 2024 abr. 26 ] - Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life
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