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Whole-Exome Sequencing Identifies Pathogenic Germline Variants in Patients with Lynch-Like Syndrome.
Dos Santos, Wellington; de Andrade, Edilene Santos; Garcia, Felipe Antonio de Oliveira; Campacci, Natália; Sábato, Cristina da Silva; Melendez, Matias Eliseo; Reis, Rui Manuel; Galvão, Henrique de Campos Reis; Palmero, Edenir Inez.
Afiliação
  • Dos Santos W; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784-400, São Paulo, Brazil.
  • de Andrade ES; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784-400, São Paulo, Brazil.
  • Garcia FAO; Laboratory of Molecular Diagnosis, Barretos Cancer Hospital, Barretos 14784-400, São Paulo, Brazil.
  • Campacci N; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784-400, São Paulo, Brazil.
  • Sábato CDS; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784-400, São Paulo, Brazil.
  • Melendez ME; Laboratory of Molecular Diagnosis, Barretos Cancer Hospital, Barretos 14784-400, São Paulo, Brazil.
  • Reis RM; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784-400, São Paulo, Brazil.
  • Galvão HCR; Department of Molecular Carcinogenesis, National Cancer Institute, Rio de Janeiro 20231-050, Rio de Janeiro, Brazil.
  • Palmero EI; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784-400, São Paulo, Brazil.
Cancers (Basel) ; 14(17)2022 Aug 31.
Article em En | MEDLINE | ID: mdl-36077770
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article