Subjects: FIBRONECTINAS, MUTAÇÃO GENÉTICA, OSTEOCONDRODISPLASIAS, DOENÇAS MUSCULOSQUELÉTICAS
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ABNT
COSTANTINI, Alice et al. Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures". Bone, v. 121, p. 163-171, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.bone.2018.12.020. Acesso em: 06 nov. 2024.APA
Costantini, A., Valta, H., Baratang, N. V., Yap, P., Bertola, D. R., Yamamoto, G. L., et al. (2019). Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures". Bone, 121, 163-171. doi:10.1016/j.bone.2018.12.020NLM
Costantini A, Valta H, Baratang NV, Yap P, Bertola DR, Yamamoto GL, Kim CA, Chen J, Wierenga KJ, Fanning EA. Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures" [Internet]. Bone. 2019 ; 121 163-171.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.bone.2018.12.020Vancouver
Costantini A, Valta H, Baratang NV, Yap P, Bertola DR, Yamamoto GL, Kim CA, Chen J, Wierenga KJ, Fanning EA. Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures" [Internet]. Bone. 2019 ; 121 163-171.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.bone.2018.12.020
