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Filtros : "MONTENEGRO, LUCIANA RIBEIRO" "Kaiser, Ursula B." Limpar

Filtros

USP affiliated authors
- mendonça, berenice bilharinho de (2)
- montenegro, luciana ribeiro (2)
- xavier, ana claudia latrônico (2)
- antonini, sonir roberto rauber (1)
- castro, margaret de (1)

Date published
- 2014 (~1)
- 2013 (~1)
Subjects
- puberdade precoce (2)
- crianças (1)
- endocrinopatias (1)
- mutação genética (1)
- transtornos do crescimento (1)

Artigo de periodico
Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 (2014)
Macedo, Delanie B.; Abreu, Ana Paula; Reis, Ana Claudia S.; Montenegro, Luciana R.; Dauber, Andrew; Beneduzzi, Daiane; Cukier, Priscilla; Silveira, Leticia F. G.; Teles, Milena G.; Carroll, Rona S.; Guerra Junior, Gil; Guaragna Filho, Guilherme; Gucev, Zoran; Arnhold, Ivo J. P.; Castro, Margaret de; Moreira, Ayrton C.; Martinelli Jr., Carlos Eduardo; Hirschhorn, Joel N.; Mendonca, Berenice B.; Brito, Vinicius N.; Antonini, Sonir R.; Kaiser, Ursula B.; Latronico, Ana Claudia
Source: Journal of Clinical Endocrinology and Metabolism. Unidades: FM, FMRP
Subjects: CRIANÇAS, TÉCNICAS GENÉTICAS, PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACEDO, Delanie B. et al. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3. Journal of Clinical Endocrinology and Metabolism, v. 99, n. 6, p. E1097-E1103, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-3126. Acesso em: 09 nov. 2024.
APA
Macedo, D. B., Abreu, A. P., Reis, A. C. S., Montenegro, L. R., Dauber, A., Beneduzzi, D., et al. (2014). Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3. Journal of Clinical Endocrinology and Metabolism, 99( 6), E1097-E1103. doi:10.1210/jc.2013-3126
NLM
Macedo DB, Abreu AP, Reis ACS, Montenegro LR, Dauber A, Beneduzzi D, Cukier P, Silveira LFG, Teles MG, Carroll RS, Guerra Junior G, Guaragna Filho G, Gucev Z, Arnhold IJP, Castro M de, Moreira AC, Martinelli Jr. CE, Hirschhorn JN, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 6): E1097-E1103.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1210/jc.2013-3126
Vancouver
Macedo DB, Abreu AP, Reis ACS, Montenegro LR, Dauber A, Beneduzzi D, Cukier P, Silveira LFG, Teles MG, Carroll RS, Guerra Junior G, Guaragna Filho G, Gucev Z, Arnhold IJP, Castro M de, Moreira AC, Martinelli Jr. CE, Hirschhorn JN, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 6): E1097-E1103.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1210/jc.2013-3126
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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