Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome (2013)
- Authors:
- USP affiliated authors: MONTENEGRO, LUCIANA RIBEIRO - FM ; XAVIER, ANA CLAUDIA LATRÔNICO - FM ; CASTRO, MARGARET DE - FMRP ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidades: FM; FMRP
- DOI: 10.1016/j.fertnstert.2013.04.045
- Subjects: SEQUENCIAMENTO GENÉTICO; AMPLIFICAÇÃO DE GENES; GENÓTIPOS; HIPOGONADISMO (GENÉTICA); DELEÇÃO DE GENES; BIOLOGIA MOLECULAR; REAÇÃO EM CADEIA POR POLIMERASE
- Language: Inglês
- Imprenta:
- Source:
- Título: Fertility and Sterility
- ISSN: 0015-0282
- Volume/Número/Paginação/Ano: v.100, n.3, p. 854-859, 2013
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
- Licença: publisher-specific-oa
-
ABNT
MONTENEGRO, Luciana Ribeiro et al. Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome. Fertility and Sterility, v. 100, n. 3, p. 854-859, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.fertnstert.2013.04.045. Acesso em: 27 dez. 2025. -
APA
Montenegro, L. R., Silveira, L. F. G., Tusset, C., Castro, M. de, Versiani, B. R., Latronico, A. C., et al. (2013). Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome. Fertility and Sterility, 100( 3), 854-859. doi:10.1016/j.fertnstert.2013.04.045 -
NLM
Montenegro LR, Silveira LFG, Tusset C, Castro M de, Versiani BR, Latronico AC, Mendonca BB, Trarbach EB. Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome [Internet]. Fertility and Sterility. 2013 ;100( 3): 854-859.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1016/j.fertnstert.2013.04.045 -
Vancouver
Montenegro LR, Silveira LFG, Tusset C, Castro M de, Versiani BR, Latronico AC, Mendonca BB, Trarbach EB. Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome [Internet]. Fertility and Sterility. 2013 ;100( 3): 854-859.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1016/j.fertnstert.2013.04.045 - Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty
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Informações sobre o DOI: 10.1016/j.fertnstert.2013.04.045 (Fonte: oaDOI API)
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