Molecular and functional characterization of variants found in DNA repair genes in a brazilian cohort with hereditary breast and ovarian cancer (2019)
- Authors:
- USP affiliated authors: MOLFETTA, GREICE ANDREOTTI DE - FMRP ; FERRAZ, VICTOR EVANGELISTA DE FARIA - FMRP ; SILVA JUNIOR, WILSON ARAÚJO DA - FMRP ; CARVALHO, SIMONE DA COSTA E SILVA - FMRP ; PLAÇA, JESSICA RODRIGUES - FMRP ; TEIXEIRA, LORENA ALVES - FMRP
- Unidade: FMRP
- Subjects: NEOPLASIAS OVARIANAS; DNA; HEREDITARIEDADE
- Keywords: HBOC; Molecular diagnosis; DNA repair genes
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher: Sociedade Brasileira de Genética
- Publisher place: Águas de Lindóia
- Date published: 2019
- Source:
- Título: Resumos
- Conference titles: Brazilian Congress of Genetics
-
ABNT
CARVALHO, Simone da Costa e Silva et al. Molecular and functional characterization of variants found in DNA repair genes in a brazilian cohort with hereditary breast and ovarian cancer. 2019, Anais.. Águas de Lindóia: Sociedade Brasileira de Genética, 2019. Disponível em: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf. Acesso em: 12 fev. 2026. -
APA
Carvalho, S. da C. e S., Brotto, D. B., Araújo, L. F. de, Teixeira, L. A., Plaça, J. R., Peronni, K. C., et al. (2019). Molecular and functional characterization of variants found in DNA repair genes in a brazilian cohort with hereditary breast and ovarian cancer. In Resumos. Águas de Lindóia: Sociedade Brasileira de Genética. Recuperado de https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf -
NLM
Carvalho S da C e S, Brotto DB, Araújo LF de, Teixeira LA, Plaça JR, Peronni KC, Molfetta GA de, Ferraz VE de F, Silva Junior WA da. Molecular and functional characterization of variants found in DNA repair genes in a brazilian cohort with hereditary breast and ovarian cancer [Internet]. Resumos. 2019 ;[citado 2026 fev. 12 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf -
Vancouver
Carvalho S da C e S, Brotto DB, Araújo LF de, Teixeira LA, Plaça JR, Peronni KC, Molfetta GA de, Ferraz VE de F, Silva Junior WA da. Molecular and functional characterization of variants found in DNA repair genes in a brazilian cohort with hereditary breast and ovarian cancer [Internet]. Resumos. 2019 ;[citado 2026 fev. 12 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf - Prediction tools for characterization of previously underscribed mutations on SLC26A4 gene in hereditary non-syndromic hearing loss patients
- Relato de caso de síndrome de Norrie por mutação gênica
- Sequenciamento do exoma sugere TWIST2 como gene causal da síndrome ablefaria macrostomia
- Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome
- Análise do gene SLC26A4 como causa da surdez neurossensorial não-sindrômica pré-lingual no sudeste brasileiro
- Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals
- Mutação "de novo" amplia o espectro de mutações da síndrome de Li-Fraumeni
- Mutation screening of the SLC26A4 gene in Brazilian nonsyndromic sensorineural prelingual deaf individuals
- Diagnóstico molecular da Síndrome de Lynch em pacientes atendidos no Ambulatório de Aconselhamento Genético do HCFMRP/USP
- Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
| 003001964.pdf |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
