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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
Source: Hormone Research in Paediatrics. Unidade: FMRP
Subjects: 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: 01 nov. 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 nov. 01 ] 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 nov. 01 ] Available from: https://doi.org/10.1159/000447515
Artigo de periodico
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome (2008)
Abreu, Ana Paula; Trarbach, Ericka Barbosa; Castro, Margaret de; Costa, Elaine Maria Frade; Versiani, Beatriz; Baptista, Maria Tereza Matias; Garmes, Heraldo Mendes; Mendonça, Berenice Bilharinho; Latronico, Ana Claudia
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Subjects: SÍNDROME DE KALLMANN, ENDOCRINOLOGIA, METABOLISMO
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 the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism, v. 93, n. 10, p. 4113-4118, 2008Tradução . . Acesso em: 01 nov. 2024.
APA
Abreu, A. P., Trarbach, E. B., Castro, M. de, Costa, E. M. F., Versiani, B., Baptista, M. T. M., et al. (2008). Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism, 93( 10), 4113-4118.
NLM
Abreu AP, Trarbach EB, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 10): 4113-4118.[citado 2024 nov. 01 ]
Vancouver
Abreu AP, Trarbach EB, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 10): 4113-4118.[citado 2024 nov. 01 ]
Trabalho de evento-resumo
Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome (2007)
Abreu, Ana Paula; Trarbach, Ericka; Castro, Margaret de; Costa, Elaine M. F.; Versiani, Beatriz; Baptista, Maria Tereza M.; Garmes, Heraldo M.; Mendonça, Berenice B.; Latronico, Ana Claudia
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting (ENDO). Unidade: FMRP
Assunto: HIPOGONADISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABREU, Ana Paula et al. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. 2007, Anais.. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2007. . Acesso em: 01 nov. 2024.
APA
Abreu, A. P., Trarbach, E., Castro, M. de, Costa, E. M. F., Versiani, B., Baptista, M. T. M., et al. (2007). Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. In Program and Abstracts. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Abreu AP, Trarbach E, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. Program and Abstracts. 2007 ;[citado 2024 nov. 01 ]
Vancouver
Abreu AP, Trarbach E, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. Program and Abstracts. 2007 ;[citado 2024 nov. 01 ]

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