ReP USP - Resultado da busca

Artigo de periodico
Usefulness of MLPA in the detection of SHOX deletions (2010)
Funari, Mariana F. A.; Jorge, Alexander A. L.; Souza, Silvia C. A. L.; Billerbeck, Ana E. C.; Arnhold, Ivo J. P.; Mendonca, Berenice B.; Nishi, Mirian Y.
Fonte: European Journal of Medical Genetics. Unidade: FM
Assuntos: PESO-ESTATURA, FENÓTIPOS, DELEÇÃO DE GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FUNARI, Mariana F. A. et al. Usefulness of MLPA in the detection of SHOX deletions. European Journal of Medical Genetics, v. 53, n. 5, p. 234-238, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2010.06.001. Acesso em: 27 abr. 2024.
APA
Funari, M. F. A., Jorge, A. A. L., Souza, S. C. A. L., Billerbeck, A. E. C., Arnhold, I. J. P., Mendonca, B. B., & Nishi, M. Y. (2010). Usefulness of MLPA in the detection of SHOX deletions. European Journal of Medical Genetics, 53( 5), 234-238. doi:10.1016/j.ejmg.2010.06.001
NLM
Funari MFA, Jorge AAL, Souza SCAL, Billerbeck AEC, Arnhold IJP, Mendonca BB, Nishi MY. Usefulness of MLPA in the detection of SHOX deletions [Internet]. European Journal of Medical Genetics. 2010 ; 53( 5): 234-238.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.ejmg.2010.06.001
Vancouver
Funari MFA, Jorge AAL, Souza SCAL, Billerbeck AEC, Arnhold IJP, Mendonca BB, Nishi MY. Usefulness of MLPA in the detection of SHOX deletions [Internet]. European Journal of Medical Genetics. 2010 ; 53( 5): 234-238.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.ejmg.2010.06.001
Artigo de periodico
Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations (2002)
Bachega, Tânia A. S. S.; Brenlha, Enecy M. L.; Billerbeck, Ana E. C.; Marcondes, José A. M.; Madureira, Guiomar; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Fonte: The Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Assuntos: ENDOCRINOLOGIA, GENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BACHEGA, Tânia A. S. S. et al. Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations. The Journal of Clinical Endocrinology & Metabolism, v. 87, n. 2, p. 786-790, 2002Tradução . . Acesso em: 27 abr. 2024.
APA
Bachega, T. A. S. S., Brenlha, E. M. L., Billerbeck, A. E. C., Marcondes, J. A. M., Madureira, G., Arnhold, I. J. P., & Mendonça, B. B. (2002). Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations. The Journal of Clinical Endocrinology & Metabolism, 87( 2), 786-790.
NLM
Bachega TASS, Brenlha EML, Billerbeck AEC, Marcondes JAM, Madureira G, Arnhold IJP, Mendonça BB. Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 2): 786-790.[citado 2024 abr. 27 ]
Vancouver
Bachega TASS, Brenlha EML, Billerbeck AEC, Marcondes JAM, Madureira G, Arnhold IJP, Mendonça BB. Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 2): 786-790.[citado 2024 abr. 27 ]
Trabalho de evento-resumo periodico
Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations (2001)
Bachega, Tania A. S. S.; Billerbeck, Ana E. C.; Madureira, Guiomar; Marcondes, Jose A. M.; Pinto, Emilia M.; Correa, Rafaela P.; Arnhold, Ivo J. P.; Mendonca, Berenice Bilharinho
Fonte: Pediatric Research. Nome do evento: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Assuntos: ENDOCRINOLOGIA, METABOLISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BACHEGA, Tania A. S. S. et al. Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2001
APA
Bachega, T. A. S. S., Billerbeck, A. E. C., Madureira, G., Marcondes, J. A. M., Pinto, E. M., Correa, R. P., et al. (2001). Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Bachega TASS, Billerbeck AEC, Madureira G, Marcondes JAM, Pinto EM, Correa RP, Arnhold IJP, Mendonca BB. Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. 2001 ; 49( 4 pt. 2): 113A. res. PI-670.[citado 2024 abr. 27 ]
Vancouver
Bachega TASS, Billerbeck AEC, Madureira G, Marcondes JAM, Pinto EM, Correa RP, Arnhold IJP, Mendonca BB. Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. 2001 ; 49( 4 pt. 2): 113A. res. PI-670.[citado 2024 abr. 27 ]

Unidades USP

ReP

Filtros

Autores

Assuntos