Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures" (2019)
- Authors:
- Autor USP: KIM, CHONG AE - FM
- Unidade: FM
- DOI: 10.1016/j.bone.2018.12.020
- Subjects: FIBRONECTINAS; MUTAÇÃO GENÉTICA; OSTEOCONDRODISPLASIAS; DOENÇAS MUSCULOSQUELÉTICAS
- Agências de fomento:
- Finnish Cultural Foundation/The Foundations' Post Doc Pool
- Financiado pelo CIHR
- Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
- Stockholm County Council
- Novo Nordisk Foundation [21322]
- Folkhalsan Research Foundation
- Sigrid Juselius Foundation
- Financiado pela AKA
- Swedish Research Council [2603]
- Language: Inglês
- Imprenta:
- Source:
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
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: 03 jun. 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.2018.12.020 -
NLM
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 jun. 03 ] Available from: https://doi.org/10.1016/j.bone.2018.12.020 -
Vancouver
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 jun. 03 ] Available from: https://doi.org/10.1016/j.bone.2018.12.020 - Caracterização clínico-laboratorial das Síndromes de Williams-Beuren e de Noonan
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Informações sobre o DOI: 10.1016/j.bone.2018.12.020 (Fonte: oaDOI API)
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