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Filtros : "MUTAÇÃO GENÉTICA" "Giugliani, Roberto" Removidos: "Indexado no: Medline" "2023" Limpar

Filtros

USP affiliated authors
- diniz, edna maria de albuquerque (~1)
- moreira filho, carlos alberto (~1)
Date published
- 2011 (~1)
- 2008 (~1)
Subjects
- mutação genética (2)
- brasil (1)
- doenças hereditárias (1)
- fatores de risco (1)
- fibrose cística (incidência) (1)

Artigo de periodico
Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome (2011)
Ewald, Ingrid P.; Izetti, Patrícia; Vargas, Fernando R.; Moreira, Miguel A. M.; Moreira, Aline S.; Moreira-Filho, Carlos A.; Cunha, Danielle R.; Hamaguchi, Sara; Camey, Suzi A.; Schmidt, Aishameriane; Caleffi, Maira; Koehler-Santos, Patrícia; Giugliani, Roberto; Ashton-Prolla, Patricia
Source: Hereditary Cancer in Clinical Practice. Unidade: FM
Subjects: NEOPLASIAS MAMÁRIAS (GENÉTICA), FATORES DE RISCO, GENES (ANÁLISE), DOENÇAS HEREDITÁRIAS, NEOPLASIAS OVARIANAS (GENÉTICA), MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
EWALD, Ingrid P. et al. Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome. Hereditary Cancer in Clinical Practice, v. 9, n. 1, p. (online), 2011Tradução . . Disponível em: https://doi.org/10.1186/1897-4287-9-12. Acesso em: 12 nov. 2024.
APA
Ewald, I. P., Izetti, P., Vargas, F. R., Moreira, M. A. M., Moreira, A. S., Moreira-Filho, C. A., et al. (2011). Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome. Hereditary Cancer in Clinical Practice, 9( 1), (online). doi:10.1186/1897-4287-9-12
NLM
Ewald IP, Izetti P, Vargas FR, Moreira MAM, Moreira AS, Moreira-Filho CA, Cunha DR, Hamaguchi S, Camey SA, Schmidt A, Caleffi M, Koehler-Santos P, Giugliani R, Ashton-Prolla P. Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome [Internet]. Hereditary Cancer in Clinical Practice. 2011 ; 9( 1): (online).[citado 2024 nov. 12 ] Available from: https://doi.org/10.1186/1897-4287-9-12
Vancouver
Ewald IP, Izetti P, Vargas FR, Moreira MAM, Moreira AS, Moreira-Filho CA, Cunha DR, Hamaguchi S, Camey SA, Schmidt A, Caleffi M, Koehler-Santos P, Giugliani R, Ashton-Prolla P. Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome [Internet]. Hereditary Cancer in Clinical Practice. 2011 ; 9( 1): (online).[citado 2024 nov. 12 ] Available from: https://doi.org/10.1186/1897-4287-9-12
Artigo de periodico
Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients (2008)
Raskin, Salmo; Ferrari, Lilian Pereira; Reis, Francisco Caldeira; Abreu, Fernando; Marostica, Paulo; Rozov, Tatiana; Cardieri, Joselina; Ludwing, Norberto; Valentin, Lairton; Rosario Filho, Nelson Augusto; Camargo Neto, Eurico; Lewis, Eduardo; Giugliani, Roberto; Diniz, Edna Maria Albuquerque; Culpi, Lodercio; Phillip III, John Atlas; Chakraborty, Ranajit
Source: Journal of cystic fibrosis. Unidade: FM
Subjects: FIBROSE CÍSTICA (INCIDÊNCIA), RASTREAMENTO, MUTAÇÃO GENÉTICA, RECÉM-NASCIDOS, PACIENTES, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RASKIN, Salmo et al. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients. Journal of cystic fibrosis, v. 7, n. 1, p. 15-22, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jcf.2007.03.006. Acesso em: 12 nov. 2024.
APA
Raskin, S., Ferrari, L. P., Reis, F. C., Abreu, F., Marostica, P., Rozov, T., et al. (2008). Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients. Journal of cystic fibrosis, 7( 1), 15-22. doi:10.1016/j.jcf.2007.03.006
NLM
Raskin S, Ferrari LP, Reis FC, Abreu F, Marostica P, Rozov T, Cardieri J, Ludwing N, Valentin L, Rosario Filho NA, Camargo Neto E, Lewis E, Giugliani R, Diniz EMA, Culpi L, Phillip III JA, Chakraborty R. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients [Internet]. Journal of cystic fibrosis. 2008 ; 7( 1): 15-22.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.jcf.2007.03.006
Vancouver
Raskin S, Ferrari LP, Reis FC, Abreu F, Marostica P, Rozov T, Cardieri J, Ludwing N, Valentin L, Rosario Filho NA, Camargo Neto E, Lewis E, Giugliani R, Diniz EMA, Culpi L, Phillip III JA, Chakraborty R. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients [Internet]. Journal of cystic fibrosis. 2008 ; 7( 1): 15-22.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.jcf.2007.03.006

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