Your browser doesn't support javascript.
loading
PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age-related clonal hematopoiesis and myeloid neoplasia.
Chase, Andrew; Pellagatti, Andrea; Singh, Shalini; Score, Joannah; Tapper, William J; Lin, Feng; Hoade, Yvette; Bryant, Catherine; Trim, Nicola; Yip, Bon Ham; Zoi, Katerina; Rasi, Chiara; Forsberg, Lars A; Dumanski, Jan P; Boultwood, Jacqueline; Cross, Nicholas C P.
Afiliação
  • Chase A; Faculty of Medicine, University of Southampton, Southampton, UK.
  • Pellagatti A; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UK.
  • Singh S; Bloodwise Molecular Haematology Unit, Nuffield Division of Clinical Laboratory Sciences, Radcliffe Department of Medicine, Oxford BRC Haematology Theme, University of Oxford, Oxford, UK.
  • Score J; Bloodwise Molecular Haematology Unit, Nuffield Division of Clinical Laboratory Sciences, Radcliffe Department of Medicine, Oxford BRC Haematology Theme, University of Oxford, Oxford, UK.
  • Tapper WJ; Faculty of Medicine, University of Southampton, Southampton, UK.
  • Lin F; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UK.
  • Hoade Y; Faculty of Medicine, University of Southampton, Southampton, UK.
  • Bryant C; Faculty of Medicine, University of Southampton, Southampton, UK.
  • Trim N; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UK.
  • Yip BH; Faculty of Medicine, University of Southampton, Southampton, UK.
  • Zoi K; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UK.
  • Rasi C; Faculty of Medicine, University of Southampton, Southampton, UK.
  • Forsberg LA; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UK.
  • Dumanski JP; West Midlands Regional Genetics Laboratory, Birmingham Women's NHS Foundation Trust, Birmingham, UK.
  • Boultwood J; Bloodwise Molecular Haematology Unit, Nuffield Division of Clinical Laboratory Sciences, Radcliffe Department of Medicine, Oxford BRC Haematology Theme, University of Oxford, Oxford, UK.
  • Cross NCP; Haematology Research Laboratory, Biomedical Research Foundation, Academy of Athens, Athens, Greece.
Leukemia ; 33(5): 1184-1194, 2019 05.
Article em En | MEDLINE | ID: mdl-30573780
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 22 / Proteínas Cromossômicas não Histona / Dissomia Uniparental / Hematopoese / Mutação / Transtornos Mieloproliferativos Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Leukemia 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: Cromossomos Humanos Par 22 / Proteínas Cromossômicas não Histona / Dissomia Uniparental / Hematopoese / Mutação / Transtornos Mieloproliferativos Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Leukemia Ano de publicação: 2019 Tipo de documento: Article