Evaluation of Mismatch repair system proficiency in endometrial cancer to detect cases of lynch syndrome: a universal approach (2017)
- Authors:
- USP affiliated authors: MARQUES JÚNIOR, WILSON - FMRP ; CHAHUD, FERNANDO - FMRP ; SILVA JUNIOR, WILSON ARAÚJO DA - FMRP ; FERRAZ, VICTOR EVANGELISTA DE FARIA - FMRP
- Unidade: FMRP
- Subjects: ENDOMÉTRIO; NEOPLASIAS
- Keywords: Hereditary endometrial cancer; Universal screening; Lynch syndrome
- Language: Inglês
- Imprenta:
- Publisher: FMRP-USP
- Publisher place: Ribeirão Preto
- Date published: 2017
- Source:
- Título: Resumos
- Conference titles: Workshop do Programa de Pós-Graduação em Genética da FMRP-USP
-
ABNT
ROSA, R. C. A. et al. Evaluation of Mismatch repair system proficiency in endometrial cancer to detect cases of lynch syndrome: a universal approach. 2017, Anais.. Ribeirão Preto: FMRP-USP, 2017. . Acesso em: 12 fev. 2026. -
APA
Rosa, R. C. A., Chahud, F., Silva, A. R., Marques Júnior, W., Marques, S. E., Souza, D. O., et al. (2017). Evaluation of Mismatch repair system proficiency in endometrial cancer to detect cases of lynch syndrome: a universal approach. In Resumos. Ribeirão Preto: FMRP-USP. -
NLM
Rosa RCA, Chahud F, Silva AR, Marques Júnior W, Marques SE, Souza DO, Silva Júnior WA da, Ferraz VE de F. Evaluation of Mismatch repair system proficiency in endometrial cancer to detect cases of lynch syndrome: a universal approach. Resumos. 2017 ;[citado 2026 fev. 12 ] -
Vancouver
Rosa RCA, Chahud F, Silva AR, Marques Júnior W, Marques SE, Souza DO, Silva Júnior WA da, Ferraz VE de F. Evaluation of Mismatch repair system proficiency in endometrial cancer to detect cases of lynch syndrome: a universal approach. Resumos. 2017 ;[citado 2026 fev. 12 ] - Detection and diagnosis of lynch syndrome and PPAP from endometrial cancer cases
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- Molecular characterization of endometrial tumors for the proficiency of the DNA-mismatch repair system
- Evaluation of mismatch repair system proficiency in endometrial cancer to detect cases of lynch syndrome: a universal approach
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- BRCA1 mutation screening in brazilian hereditary breast cancer and ovary syndrome using high resolution melting
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