Source: American Journal of Medical Genetics Part A. Unidades: IB, FM
Subjects: MUTAÇÃO GENÉTICA, RECIDIVA, DIAGNÓSTICO POR COMPUTADOR, OSTEOCONDRODISPLASIAS
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SILVEIRA, Karina C. et al. Six additional cases of SEDC due to the same and recurrent R989C mutation in the COL2A1 gene—the clinical and radiological follow-up [Carta]. American Journal of Medical Genetics Part A. Hoboken: Instituto de Biociências, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.36954/epdf. Acesso em: 23 maio 2024. , 2015APA
Silveira, K. C., Bonadia, L. C., Superti-Furga, A., Bertola, D. R., Jorge, A. A. L., & Cavalcanti, D. P. (2015). Six additional cases of SEDC due to the same and recurrent R989C mutation in the COL2A1 gene—the clinical and radiological follow-up [Carta]. American Journal of Medical Genetics Part A. Hoboken: Instituto de Biociências, Universidade de São Paulo. doi:10.1002/ajmg.a.36954NLM
Silveira KC, Bonadia LC, Superti-Furga A, Bertola DR, Jorge AAL, Cavalcanti DP. Six additional cases of SEDC due to the same and recurrent R989C mutation in the COL2A1 gene—the clinical and radiological follow-up [Carta] [Internet]. American Journal of Medical Genetics Part A. 2015 ;( 4): 894-901.[citado 2024 maio 23 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.36954/epdfVancouver
Silveira KC, Bonadia LC, Superti-Furga A, Bertola DR, Jorge AAL, Cavalcanti DP. Six additional cases of SEDC due to the same and recurrent R989C mutation in the COL2A1 gene—the clinical and radiological follow-up [Carta] [Internet]. American Journal of Medical Genetics Part A. 2015 ;( 4): 894-901.[citado 2024 maio 23 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.36954/epdf
