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Artigo de periodico
Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing (2017)
Correa, Fernanda A.; França, Marcela M; Fang, Qing; Ma, Qianyi; Bachega, Tânia Aparecida Sartori Sanchez; Rodrigues, Andresa; Ozel, Bilge A; Li, Jun Z; Mendonça, Berenice Bilharinho de; Jorge, Alexander Augusto de Lima; Carvalho, Luciani R; Camper, Sally A; Arnhold, Ivo J
Source: Archives of endocrinology metabolism. Unidade: FM
Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA, HORMÔNIO DO CRESCIMENTO, DOENÇAS DO DESENVOLVIMENTO ÓSSEO
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ABNT
CORREA, Fernanda A. et al. Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing. Archives of endocrinology metabolism, v. 61, n. 6, p. 633-636, 2017Tradução . . Disponível em: https://doi.org/10.1590/2359-3997000000311. Acesso em: 02 maio 2024.
APA
Correa, F. A., França, M. M., Fang, Q., Ma, Q., Bachega, T. A. S. S., Rodrigues, A., et al. (2017). Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing. Archives of endocrinology metabolism, 61( 6), 633-636. doi:10.1590/2359-3997000000311
NLM
Correa FA, França MM, Fang Q, Ma Q, Bachega TASS, Rodrigues A, Ozel BA, Li JZ, Mendonça BB de, Jorge AA de L, Carvalho LR, Camper SA, Arnhold IJ. Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing [Internet]. Archives of endocrinology metabolism. 2017 ; 61( 6): 633-636.[citado 2024 maio 02 ] Available from: https://doi.org/10.1590/2359-3997000000311
Vancouver
Correa FA, França MM, Fang Q, Ma Q, Bachega TASS, Rodrigues A, Ozel BA, Li JZ, Mendonça BB de, Jorge AA de L, Carvalho LR, Camper SA, Arnhold IJ. Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing [Internet]. Archives of endocrinology metabolism. 2017 ; 61( 6): 633-636.[citado 2024 maio 02 ] Available from: https://doi.org/10.1590/2359-3997000000311
Trabalho de evento-resumo periodico
Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life (2017)
Ramos, Carolina O; Xavier, Ana Claudia Latronico; Cukier, Priscila; Cukier, Priscila; Macedo, Delaine; Bessa, Danielle S; Silva, Marina C; Arnhold, Ivo J; Mendonça, Berenice Bilharinho de; Brito, Vinicius N
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: PUBERDADE PRECOCE, NEOPLASIAS, HIPOTÁLAMO, HORMÔNIO LIBERADOR DE GONADOTROFINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Carolina O et al. Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 02 maio 2024. , 2017
APA
Ramos, C. O., Xavier, A. C. L., Cukier, P., Cukier, P., Macedo, D., Bessa, D. S., et al. (2017). Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Ramos CO, Xavier ACL, Cukier P, Cukier P, Macedo D, Bessa DS, Silva MC, Arnhold IJ, Mendonça BB de, Brito VN. Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life. Hormone research in paediatrics. 2017 ; 88 351-352.[citado 2024 maio 02 ]
Vancouver
Ramos CO, Xavier ACL, Cukier P, Cukier P, Macedo D, Bessa DS, Silva MC, Arnhold IJ, Mendonça BB de, Brito VN. Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life. Hormone research in paediatrics. 2017 ; 88 351-352.[citado 2024 maio 02 ]
Trabalho de evento-resumo
Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis (2004)
Melo, Maria E; Marui, Suemi; Gomes, Miriam C; Arnhold, Ivo J; Mendonça, Berenice Bilharinho de; Knopfelmacher, Mirta
Source: Program and Abstracts. Conference titles: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: DIFERENCIAÇÃO CELULCAR, MUTAÇÃO GENÉTICA, POLIMORFISMO, HIPÓFISE (ANORMALIDADES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Maria E et al. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 02 maio 2024.
APA
Melo, M. E., Marui, S., Gomes, M. C., Arnhold, I. J., Mendonça, B. B. de, & Knopfelmacher, M. (2004). Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
Melo ME, Marui S, Gomes MC, Arnhold IJ, Mendonça BB de, Knopfelmacher M. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. Program and Abstracts. 2004 ;[citado 2024 maio 02 ]
Vancouver
Melo ME, Marui S, Gomes MC, Arnhold IJ, Mendonça BB de, Knopfelmacher M. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. Program and Abstracts. 2004 ;[citado 2024 maio 02 ]

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