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Filtros : "Dutra, Roberta Lelis" "Dias, Alexandre Torchio" Removido: "Campos, Carla Marques Rondon" Limpar

Filtros

Artigo de periodico
Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience (2017)
Zanardo, Évelin Aline; Dutra, Roberta Lelis; Piazzon, Flavia Balbo; Dias, Alexandre Torchio; Novo-Filho, Gil Monteiro; Nascimento, Amom Mendes; Montenegro, Marília Moreira; Damasceno, Jullian Gabriel; Madia, Fabrícia Andreia Rosa; Costa, Thaís Virgínia Moura Machado da; Melaragno, Maria Isabel; Kim, Chong Ae; Kulikowski, Leslie Domenici
Source: Clinics. Unidade: FM
Subjects: CRIANÇAS, ANORMALIDADES MÚLTIPLAS, REAÇÃO EM CADEIA POR POLIMERASE, DIAGNÓSTICO, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZANARDO, Évelin Aline et al. Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience. Clinics, v. 72, n. 9, p. 526-537, 2017Tradução . . Disponível em: https://doi.org/10.6061/clinics/2017(09)02. Acesso em: 10 ago. 2024.
APA
Zanardo, É. A., Dutra, R. L., Piazzon, F. B., Dias, A. T., Novo-Filho, G. M., Nascimento, A. M., et al. (2017). Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience. Clinics, 72( 9), 526-537. doi:10.6061/clinics/2017(09)02
NLM
Zanardo ÉA, Dutra RL, Piazzon FB, Dias AT, Novo-Filho GM, Nascimento AM, Montenegro MM, Damasceno JG, Madia FAR, Costa TVMM da, Melaragno MI, Kim CA, Kulikowski LD. Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience [Internet]. Clinics. 2017 ; 72( 9): 526-537.[citado 2024 ago. 10 ] Available from: https://doi.org/10.6061/clinics/2017(09)02
Vancouver
Zanardo ÉA, Dutra RL, Piazzon FB, Dias AT, Novo-Filho GM, Nascimento AM, Montenegro MM, Damasceno JG, Madia FAR, Costa TVMM da, Melaragno MI, Kim CA, Kulikowski LD. Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience [Internet]. Clinics. 2017 ; 72( 9): 526-537.[citado 2024 ago. 10 ] Available from: https://doi.org/10.6061/clinics/2017(09)02
Artigo de periodico
Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome (2014)
Zanardo, Évelin Aline; Piazzon, Flavia Balbo; Dutra, Roberta Lelis; Dias, Alexandre Torchio; Montenegro, Marília Moreira; Novo-Filho, Gil Monteiro; Costa, Thaís Virgínia Moura Machado; Nascimento, Amom Mendes; Kim, Chong Ae; Kulikowski, Leslie Domenici
Source: Molecular genetics and genomics. Unidade: FM
Subjects: DOENÇAS HEREDITÁRIAS, TÉCNICAS BIOLÓGICAS, REPARAÇÃO DE DNA, CROMOSSOMOS (ANORMALIDADES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZANARDO, Évelin Aline et al. Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome. Molecular genetics and genomics, v. 289, n. 6, p. 1037-1043, 2014Tradução . . Disponível em: https://doi.org/10.1007/s00438-014-0876-7. Acesso em: 10 ago. 2024.
APA
Zanardo, É. A., Piazzon, F. B., Dutra, R. L., Dias, A. T., Montenegro, M. M., Novo-Filho, G. M., et al. (2014). Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome. Molecular genetics and genomics, 289( 6), 1037-1043. doi:10.1007/s00438-014-0876-7
NLM
Zanardo ÉA, Piazzon FB, Dutra RL, Dias AT, Montenegro MM, Novo-Filho GM, Costa TVMM, Nascimento AM, Kim CA, Kulikowski LD. Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome [Internet]. Molecular genetics and genomics. 2014 ; 289( 6): 1037-1043.[citado 2024 ago. 10 ] Available from: https://doi.org/10.1007/s00438-014-0876-7
Vancouver
Zanardo ÉA, Piazzon FB, Dutra RL, Dias AT, Montenegro MM, Novo-Filho GM, Costa TVMM, Nascimento AM, Kim CA, Kulikowski LD. Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome [Internet]. Molecular genetics and genomics. 2014 ; 289( 6): 1037-1043.[citado 2024 ago. 10 ] Available from: https://doi.org/10.1007/s00438-014-0876-7

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