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Artigo de periodico
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty (2017)
Dauber, Andrew; Cunha-Silva, Marina; Macedo, Delanie B.; Brito, Vinicius N.; Abreu, Ana Paula; Roberts, Stephanie A.; Montenegro, Luciana R.; Andrew, Melissa; Kirby, Andrew; Weirauch, Matthew T.; Labilloy, Guillaume; Bessa, Danielle S.; Carroll, Rona S.; Jacobs, Dakota C.; Chappell, Patrick E.; Mendonca, Berenice B.; Haig, David; Kaiser, Ursula B.; Latronico, Ana Claudia
Fonte: Journal of clinical endocrinology and metabolism. Unidade: FM
Assuntos: PUBERDADE PRECOCE, REAÇÃO EM CADEIA POR POLIMERASE, HIPOTÁLAMO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DAUBER, Andrew et al. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. Journal of clinical endocrinology and metabolism, v. 102, n. 5, p. 1557-1567, 2017Tradução . . Disponível em: https://doi.org/10.1210/jc.2016-3677. Acesso em: 02 out. 2024.
APA
Dauber, A., Cunha-Silva, M., Macedo, D. B., Brito, V. N., Abreu, A. P., Roberts, S. A., et al. (2017). Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. Journal of clinical endocrinology and metabolism, 102( 5), 1557-1567. doi:10.1210/jc.2016-3677
NLM
Dauber A, Cunha-Silva M, Macedo DB, Brito VN, Abreu AP, Roberts SA, Montenegro LR, Andrew M, Kirby A, Weirauch MT, Labilloy G, Bessa DS, Carroll RS, Jacobs DC, Chappell PE, Mendonca BB, Haig D, Kaiser UB, Latronico AC. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology and metabolism. 2017 ; 102( 5): 1557-1567.[citado 2024 out. 02 ] Available from: https://doi.org/10.1210/jc.2016-3677
Vancouver
Dauber A, Cunha-Silva M, Macedo DB, Brito VN, Abreu AP, Roberts SA, Montenegro LR, Andrew M, Kirby A, Weirauch MT, Labilloy G, Bessa DS, Carroll RS, Jacobs DC, Chappell PE, Mendonca BB, Haig D, Kaiser UB, Latronico AC. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology and metabolism. 2017 ; 102( 5): 1557-1567.[citado 2024 out. 02 ] Available from: https://doi.org/10.1210/jc.2016-3677
Artigo de periodico
Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care (2016)
Stecchini, Monica F.; Macedo, Delanie B.; Reis, Ana Claudia S.; Abreu, Ana Paula; Moreira, Ayrton Custódio; Castro, Margaret de; Kaiser, Ursula B.; Latronico, Ana Claudia; Antonini, Sonir Roberto Rauber
Fonte: Hormone Research in Paediatrics. Unidade: FMRP
Assuntos: PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA, AMINOÁCIDOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STECCHINI, Monica F. et al. Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care. Hormone Research in Paediatrics, v. 86, n. 2, p. 126-130, 2016Tradução . . Disponível em: https://doi.org/10.1159/000447515. Acesso em: 02 out. 2024.
APA
Stecchini, M. F., Macedo, D. B., Reis, A. C. S., Abreu, A. P., Moreira, A. C., Castro, M. de, et al. (2016). Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care. Hormone Research in Paediatrics, 86( 2), 126-130. doi:10.1159/000447515
NLM
Stecchini MF, Macedo DB, Reis ACS, Abreu AP, Moreira AC, Castro M de, Kaiser UB, Latronico AC, Antonini SRR. Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care [Internet]. Hormone Research in Paediatrics. 2016 ; 86( 2): 126-130.[citado 2024 out. 02 ] Available from: https://doi.org/10.1159/000447515
Vancouver
Stecchini MF, Macedo DB, Reis ACS, Abreu AP, Moreira AC, Castro M de, Kaiser UB, Latronico AC, Antonini SRR. Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care [Internet]. Hormone Research in Paediatrics. 2016 ; 86( 2): 126-130.[citado 2024 out. 02 ] Available from: https://doi.org/10.1159/000447515
Artigo de periodico
A new pathway in the control of the initiation of puberty: the MKRN3 gene (2015)
Abreu, Ana Paula; Macedo, Delanie B.; Brito, Vinicius N.; Kaiser, Ursula B.; Latronico, Ana Claudia
Fonte: Journal of Molecular Endocrinology. Unidade: FM
Assuntos: SECREÇÃO, PUBERDADE, HIPOTÁLAMO, GONADOTROFINAS, ESTÁGIOS DE DESENVOLVIMENTO, NEUROENDOCRINOLOGIA, MUTAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABREU, Ana Paula et al. A new pathway in the control of the initiation of puberty: the MKRN3 gene. Journal of Molecular Endocrinology, v. 54, n. 3, p. R131-R139, 2015Tradução . . Disponível em: https://doi.org/10.1530/JME-14-0315. Acesso em: 02 out. 2024.
APA
Abreu, A. P., Macedo, D. B., Brito, V. N., Kaiser, U. B., & Latronico, A. C. (2015). A new pathway in the control of the initiation of puberty: the MKRN3 gene. Journal of Molecular Endocrinology, 54( 3), R131-R139. doi:10.1530/JME-14-0315
NLM
Abreu AP, Macedo DB, Brito VN, Kaiser UB, Latronico AC. A new pathway in the control of the initiation of puberty: the MKRN3 gene [Internet]. Journal of Molecular Endocrinology. 2015 ; 54( 3): R131-R139.[citado 2024 out. 02 ] Available from: https://doi.org/10.1530/JME-14-0315
Vancouver
Abreu AP, Macedo DB, Brito VN, Kaiser UB, Latronico AC. A new pathway in the control of the initiation of puberty: the MKRN3 gene [Internet]. Journal of Molecular Endocrinology. 2015 ; 54( 3): R131-R139.[citado 2024 out. 02 ] Available from: https://doi.org/10.1530/JME-14-0315
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
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidades: FM, FMRP
Assuntos: 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: 02 out. 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 out. 02 ] 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 out. 02 ] Available from: https://doi.org/10.1210/jc.2013-3126
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.
Fonte: The New England Journal of Medicine. Unidade: FM
Assuntos: 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: 02 out. 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 out. 02 ] 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 out. 02 ] Available from: http://www.nejm.org/doi/full/10.1056/NEJMoa1302160

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