Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Unidade: FM
Subjects: DELEÇÃO DE GENES, DOENÇAS HEREDITÁRIAS, DOENÇAS GENÉTICAS, AMPLIFICAÇÃO DE GENES, GENOMAS
ABNT
FUNARI, Mariana F. A. et al. Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA). Arquivos Brasileiros de Endocrinologia e Metabologia, v. 52, n. 8, p. 1382-1387, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302008000800029. Acesso em: 30 set. 2024.APA
Funari, M. F. A., Jorge, A. A. L., Pinto, E. M., Arnhold, I. J. P., Mendonca, B. B., & Nishi, M. Y. (2008). Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA). Arquivos Brasileiros de Endocrinologia e Metabologia, 52( 8), 1382-1387. doi:10.1590/s0004-27302008000800029NLM
Funari MFA, Jorge AAL, Pinto EM, Arnhold IJP, Mendonca BB, Nishi MY. Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA) [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52( 8): 1382-1387.[citado 2024 set. 30 ] Available from: https://doi.org/10.1590/s0004-27302008000800029Vancouver
Funari MFA, Jorge AAL, Pinto EM, Arnhold IJP, Mendonca BB, Nishi MY. Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA) [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52( 8): 1382-1387.[citado 2024 set. 30 ] Available from: https://doi.org/10.1590/s0004-27302008000800029