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Artigo de periodico
Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature (2022)
Andrade, Nathalia Liberatoscioli Menezes; Funari, Mariana Ferreira de Assis; Scalco, Renata; Dantas, Naiara Castelo Branc; Rezende, Raissa C; Freire, Bruna L; Krepischi, Ana Cristina Victorino ; Arnhold, Ivo J P; Jorge, Alexander A. L; Vasques, Gabriela Andrade
Source: Endocrine Connections. Unidades: IB, FM
Subjects: MUTAÇÃO GENÉTICA, SEQUENCIAMENTO GENÉTICO, CRIANÇAS, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANDRADE, Nathalia Liberatoscioli Menezes et al. Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature. Endocrine Connections, v. 11, n. 12, 2022Tradução . . Disponível em: https://doi.org/10.1530/EC-22-0214. Acesso em: 01 nov. 2024.
APA
Andrade, N. L. M., Funari, M. F. de A., Scalco, R., Dantas, N. C. B., Rezende, R. C., Freire, B. L., et al. (2022). Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature. Endocrine Connections, 11( 12). doi:10.1530/EC-22-0214
NLM
Andrade NLM, Funari MF de A, Scalco R, Dantas NCB, Rezende RC, Freire BL, Krepischi ACV, Arnhold IJP, Jorge AAL, Vasques GA. Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature [Internet]. Endocrine Connections. 2022 ; 11( 12):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1530/EC-22-0214
Vancouver
Andrade NLM, Funari MF de A, Scalco R, Dantas NCB, Rezende RC, Freire BL, Krepischi ACV, Arnhold IJP, Jorge AAL, Vasques GA. Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature [Internet]. Endocrine Connections. 2022 ; 11( 12):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1530/EC-22-0214
Artigo de periodico
Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature (2020)
Homma, Thais K; Freire, Bruna L; Honjo, Rachel; Dauber, Andrew; Funari, Mariana F. A; Lerario, Antonio M; Albuquerque, Edoarda V. A; Vasques, Gabriela A; Bertola, Debora R; Kim, Chong Ae ; Jorge, Alexander Augusto de Lima
Source: Hormone research in paediatrics. Unidade: FM
Subjects: EXONS, TERAPÊUTICA, CRESCIMENTO, HORMÔNIO DO CRESCIMENTO, MUTAÇÃO, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HOMMA, Thais K et al. Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature. Hormone research in paediatrics, v. 92, n. 2, p. 115-123, 2020Tradução . . Disponível em: https://doi.org/10.1159/000503782. Acesso em: 01 nov. 2024.
APA
Homma, T. K., Freire, B. L., Honjo, R., Dauber, A., Funari, M. F. A., Lerario, A. M., et al. (2020). Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature. Hormone research in paediatrics, 92( 2), 115-123. doi:10.1159/000503782
NLM
Homma TK, Freire BL, Honjo R, Dauber A, Funari MFA, Lerario AM, Albuquerque EVA, Vasques GA, Bertola DR, Kim CA, Jorge AA de L. Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature [Internet]. Hormone research in paediatrics. 2020 ; 92( 2): 115-123.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1159/000503782
Vancouver
Homma TK, Freire BL, Honjo R, Dauber A, Funari MFA, Lerario AM, Albuquerque EVA, Vasques GA, Bertola DR, Kim CA, Jorge AA de L. Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature [Internet]. Hormone research in paediatrics. 2020 ; 92( 2): 115-123.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1159/000503782
Artigo de periodico
Evaluation of SHOX defects in the era of next-generation sequencing (2019)
Funari, Mariana F. A; Barros, Juliana S. de; Santana, Lucas S; Lerario, Antonio M; Freire, Bruna L; Homma, Thais K; Vasques, Gabriela A; Mendonça, Berenice Bilharinho de ; Nishi, Mirian Y; Jorge, Alexander Augusto de Lima
Source: Clinical genetics. Unidade: FM
Subjects: GENES HOMEOBOX, MUTAÇÃO, INSUFICIÊNCIA DE CRESCIMENTO, GENÔMICA, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FUNARI, Mariana F. A et al. Evaluation of SHOX defects in the era of next-generation sequencing. Clinical genetics, v. 96, n. 3, p. 261-265, 2019Tradução . . Disponível em: https://doi.org/10.1111/cge.13587. Acesso em: 01 nov. 2024.
APA
Funari, M. F. A., Barros, J. S. de, Santana, L. S., Lerario, A. M., Freire, B. L., Homma, T. K., et al. (2019). Evaluation of SHOX defects in the era of next-generation sequencing. Clinical genetics, 96( 3), 261-265. doi:10.1111/cge.13587
NLM
Funari MFA, Barros JS de, Santana LS, Lerario AM, Freire BL, Homma TK, Vasques GA, Mendonça BB de, Nishi MY, Jorge AA de L. Evaluation of SHOX defects in the era of next-generation sequencing [Internet]. Clinical genetics. 2019 ; 96( 3): 261-265.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1111/cge.13587
Vancouver
Funari MFA, Barros JS de, Santana LS, Lerario AM, Freire BL, Homma TK, Vasques GA, Mendonça BB de, Nishi MY, Jorge AA de L. Evaluation of SHOX defects in the era of next-generation sequencing [Internet]. Clinical genetics. 2019 ; 96( 3): 261-265.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1111/cge.13587
Artigo de periodico
Multigene sequencing analysis of children born small for gestational age with isolated short stature (2019)
Freire, Bruna L; Homma, Thais K.; Funari, Mariana F. A.; Lerario, Antonio M.; Vasques, Gabriela A.; Malaquias, Alexsandra C.; Arnhold, Ivo J. P.; Jorge, Alexander Augusto de Lima
Source: Journal of clinical endocrinology & metabolism. Unidade: FM
Subjects: TRANSTORNOS DO CRESCIMENTO, RECÉM-NASCIDO PEQUENO PARA IDADE GESTACIONAL, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREIRE, Bruna L et al. Multigene sequencing analysis of children born small for gestational age with isolated short stature. Journal of clinical endocrinology & metabolism, v. 104, n. 6, p. 2023-2030, 2019Tradução . . Disponível em: https://doi.org/10.1210/jc.2018-01971. Acesso em: 01 nov. 2024.
APA
Freire, B. L., Homma, T. K., Funari, M. F. A., Lerario, A. M., Vasques, G. A., Malaquias, A. C., et al. (2019). Multigene sequencing analysis of children born small for gestational age with isolated short stature. Journal of clinical endocrinology & metabolism, 104( 6), 2023-2030. doi:10.1210/jc.2018-01971
NLM
Freire BL, Homma TK, Funari MFA, Lerario AM, Vasques GA, Malaquias AC, Arnhold IJP, Jorge AA de L. Multigene sequencing analysis of children born small for gestational age with isolated short stature [Internet]. Journal of clinical endocrinology & metabolism. 2019 ; 104( 6): 2023-2030.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/jc.2018-01971
Vancouver
Freire BL, Homma TK, Funari MFA, Lerario AM, Vasques GA, Malaquias AC, Arnhold IJP, Jorge AA de L. Multigene sequencing analysis of children born small for gestational age with isolated short stature [Internet]. Journal of clinical endocrinology & metabolism. 2019 ; 104( 6): 2023-2030.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/jc.2018-01971
Artigo de periodico
Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patients (2019)
Villela, Thais R; Freire, Bruna L; Braga, Nathalia T. P; Arantes, Rodrigo R; Funari, Mariana F. A; Jorge, Alexander Augusto de Lima ; Silva, Ivani N
Source: Genetics and molecular biology. Unidade: FM
Subjects: NANISMO, HORMÔNIO DO CRESCIMENTO, FATOR DE CRESCIMENTO INSULIN-LIKE I, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILLELA, Thais R et al. Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patients. Genetics and molecular biology, v. 42, n. 4, 2019Tradução . . Disponível em: https://doi.org/10.1590/1678-4685-GMB-2018-0197. Acesso em: 01 nov. 2024.
APA
Villela, T. R., Freire, B. L., Braga, N. T. P., Arantes, R. R., Funari, M. F. A., Jorge, A. A. de L., & Silva, I. N. (2019). Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patients. Genetics and molecular biology, 42( 4). doi:10.1590/1678-4685-GMB-2018-0197
NLM
Villela TR, Freire BL, Braga NTP, Arantes RR, Funari MFA, Jorge AA de L, Silva IN. Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patients [Internet]. Genetics and molecular biology. 2019 ; 42( 4):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1590/1678-4685-GMB-2018-0197
Vancouver
Villela TR, Freire BL, Braga NTP, Arantes RR, Funari MFA, Jorge AA de L, Silva IN. Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patients [Internet]. Genetics and molecular biology. 2019 ; 42( 4):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1590/1678-4685-GMB-2018-0197

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