Your browser doesn't support javascript.
loading
Further evidence that full gene deletions of DICER1 predispose to DICER1 syndrome.
de Kock, Leanne; Hillmer, Morten; Wagener, Rabea; Soglio, Dorothée Bouron-Dal; Sabbaghian, Nelly; Siebert, Reiner; Priest, John R; Miller, Michal; Foulkes, William D.
Afiliação
  • de Kock L; Department of Human Genetics, McGill University, Montréal, Québec, Canada.
  • Hillmer M; Lady Davis Institute, Segal Cancer Centre, Jewish General Hospital, Montréal, Québec, Canada.
  • Wagener R; Institute of Human Genetics, Ulm University and Ulm University Medical Centre, Ulm, Germany.
  • Soglio DB; Institute of Human Genetics, Ulm University and Ulm University Medical Centre, Ulm, Germany.
  • Sabbaghian N; Department of Pathology, CHU Sainte Justine, Montréal, Québec, Canada.
  • Siebert R; Department of Pathology and Cellular Biology, Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada.
  • Priest JR; Lady Davis Institute, Segal Cancer Centre, Jewish General Hospital, Montréal, Québec, Canada.
  • Miller M; Institute of Human Genetics, Ulm University and Ulm University Medical Centre, Ulm, Germany.
  • Foulkes WD; Minneapolis, Minnesota.
Genes Chromosomes Cancer ; 58(8): 602-604, 2019 08.
Article em En | MEDLINE | ID: mdl-30597651
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Deleção de Genes / Ribonuclease III / RNA Helicases DEAD-box Limite: Adolescent / Female / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Deleção de Genes / Ribonuclease III / RNA Helicases DEAD-box Limite: Adolescent / Female / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article