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Filtros : "Gill, John C." Limpar

Filtros

USP affiliated authors
- mendonça, berenice bilharinho de (~2)
- xavier, ana claudia latrônico (~2)
- montenegro, luciana ribeiro (~1)
Date published
- 2013 (~2)
Subjects
- puberdade precoce (2)
- análise sequencial (1)
- biologia molecular (1)
- endocrinopatias (1)
- gonadotrofinas (1)

Artigo de periodico
Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3 (2013)
Abreu, Ana Paula; Dauber, Andrew; Macedo, Delanie B.; Noel, Sekoni D.; Brito, Vinicius N.; Gill, John C.; Cukier, Priscilla; Thompson, Iain R.; Navarro, Victor M.; Gagliardi, Priscila C.; Rodrigues, Tânia; Kochi, Cristiane; Longui, Carlos Alberto; Beckers, Dominique; Zegher, Francis de; Montenegro, Luciana R.; Mendonca, Berenice B.; Carroll, Rona S.; Hirschhorn, Joel N.; Latronico, Ana Claudia; Kaiser, Ursula B.
Source: The New England Journal of Medicine. Unidade: FM
Subjects: PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA, GONADOTROFINAS, REAÇÃO EM CADEIA POR POLIMERASE, BIOLOGIA MOLECULAR, ANÁLISE SEQUENCIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABREU, Ana Paula et al. Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3. The New England Journal of Medicine, v. 368, n. 26, p. 2467-2475, 2013Tradução . . Disponível em: http://www.nejm.org/doi/full/10.1056/NEJMoa1302160. Acesso em: 09 nov. 2024.
APA
Abreu, A. P., Dauber, A., Macedo, D. B., Noel, S. D., Brito, V. N., Gill, J. C., et al. (2013). Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3. The New England Journal of Medicine, 368( 26), 2467-2475. doi:10.1056/NEJMoa1302160
NLM
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson IR, Navarro VM, Gagliardi PC, Rodrigues T, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonca BB, Carroll RS, Hirschhorn JN, Latronico AC, Kaiser UB. Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3 [Internet]. The New England Journal of Medicine. 2013 ; 368( 26): 2467-2475.[citado 2024 nov. 09 ] Available from: http://www.nejm.org/doi/full/10.1056/NEJMoa1302160
Vancouver
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson IR, Navarro VM, Gagliardi PC, Rodrigues T, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonca BB, Carroll RS, Hirschhorn JN, Latronico AC, Kaiser UB. Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3 [Internet]. The New England Journal of Medicine. 2013 ; 368( 26): 2467-2475.[citado 2024 nov. 09 ] Available from: http://www.nejm.org/doi/full/10.1056/NEJMoa1302160
Trabalho de evento-resumo periodico
Loss-of-function mutations in a gene cause central precocius puberty (2013)
Abreu, Ana Paula; Dauber, Andrew; Macedo, Delaine Bulcão; Noel, Sekoni D.; Brito, Vinicius Nahime; Gill, John C.; Cukier, Priscilla; Thompson, Ian; Navarro, Victor M.; Gagliardi, Priscila C.; Rodrigues, Tânia M.; Kochi, Cristiane; Longui, Carlos A.; Beckers, Dominique; Zegher, Francis de; Montenegro, Luciana R.; Mendonça, Berenice Bilharinho de; Carroll, Rona S.; Hirschhorn, Joel N.; Xavier, Ana Claudia Latronico; Kaiser, Ursula B.
Source: Hormone Research in Paediatrics. Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Subjects: PUBERDADE PRECOCE, TRANSTORNOS DO CRESCIMENTO, ENDOCRINOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABREU, Ana Paula et al. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 09 nov. 2024. , 2013
APA
Abreu, A. P., Dauber, A., Macedo, D. B., Noel, S. D., Brito, V. N., Gill, J. C., et al. (2013). Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson I, Navarro VM, Gagliardi PC, Rodrigues TM, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonça BB de, Carroll RS, Hirschhorn JN, Xavier ACL, Kaiser UB. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. 2013 ; 80 35.[citado 2024 nov. 09 ]
Vancouver
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson I, Navarro VM, Gagliardi PC, Rodrigues TM, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonça BB de, Carroll RS, Hirschhorn JN, Xavier ACL, Kaiser UB. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. 2013 ; 80 35.[citado 2024 nov. 09 ]

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