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Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies.
Nelson, Dominic; Moreau, Claudia; de Vriendt, Marianne; Zeng, Yixiao; Preuss, Christoph; Vézina, Hélène; Milot, Emmanuel; Andelfinger, Gregor; Labuda, Damian; Gravel, Simon.
Afiliação
  • Nelson D; McGill University and Genome Quebec Innovation Centre, Montréal, QC H3A 0G1, Canada.
  • Moreau C; Centre Hospitalier Universitaire Sainte-Justine Research Centre, Pediatrics Department, Université de Montréal, Montréal, QC H3T 1C5, Canada.
  • de Vriendt M; McGill University and Genome Quebec Innovation Centre, Montréal, QC H3A 0G1, Canada; Biology Department, École polytechnique, 91120 Palaiseau Cedex, France.
  • Zeng Y; McGill University and Genome Quebec Innovation Centre, Montréal, QC H3A 0G1, Canada; Lady Davis Research Institute, Jewish General Hospital, Montréal, QC H3T 1E2, Canada.
  • Preuss C; Centre Hospitalier Universitaire Sainte-Justine Research Centre, Pediatrics Department, Université de Montréal, Montréal, QC H3T 1C5, Canada; The Jackson Laboratory, Bar Harbor, ME 04609, USA.
  • Vézina H; BALSAC Project, Université du Québec à Chicoutimi, Chicoutimi, QC G7H 2B1, Canada.
  • Milot E; Chemistry, Biochemistry and Physics Department, and Forensic Research Group, Université du Québec à Trois-Rivières, Trois-Rivières, QC G9A 5H7, Canada.
  • Andelfinger G; Centre Hospitalier Universitaire Sainte-Justine Research Centre, Pediatrics Department, Université de Montréal, Montréal, QC H3T 1C5, Canada.
  • Labuda D; Centre Hospitalier Universitaire Sainte-Justine Research Centre, Pediatrics Department, Université de Montréal, Montréal, QC H3T 1C5, Canada.
  • Gravel S; McGill University and Genome Quebec Innovation Centre, Montréal, QC H3A 0G1, Canada. Electronic address: simon.gravel@mcgill.ca.
Am J Hum Genet ; 103(6): 893-906, 2018 12 06.
Article em En | MEDLINE | ID: mdl-30526866
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Raras / Grupos Populacionais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: America do norte Idioma: En Revista: Am J Hum Genet Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Raras / Grupos Populacionais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: America do norte Idioma: En Revista: Am J Hum Genet Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá