Your browser doesn't support javascript.
loading
Impact of TP53 mutation variant allele frequency on phenotype and outcomes in myelodysplastic syndromes.
Sallman, D A; Komrokji, R; Vaupel, C; Cluzeau, T; Geyer, S M; McGraw, K L; Al Ali, N H; Lancet, J; McGinniss, M J; Nahas, S; Smith, A E; Kulasekararaj, A; Mufti, G; List, A; Hall, J; Padron, E.
Afiliação
  • Sallman DA; Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Komrokji R; Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Vaupel C; Genoptix, Inc., a Novartis company, Carlsbad, CA, USA.
  • Cluzeau T; Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Geyer SM; Hematology Department, CHU of Nice, Nice, France.
  • McGraw KL; Faculty of Medicine, University Nice Sophia Antipolis, Nice, France.
  • Al Ali NH; Mediterranean Center of Molecular Medicine, INSERM U1065, Nice, France.
  • Lancet J; French Group of Myelodysplasia, Paris, France.
  • McGinniss MJ; Health Informatics Institute, University of South Florida, Tampa, FL, USA.
  • Nahas S; Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Smith AE; Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Kulasekararaj A; Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Mufti G; Genoptix, Inc., a Novartis company, Carlsbad, CA, USA.
  • List A; Genoptix, Inc., a Novartis company, Carlsbad, CA, USA.
  • Hall J; King's College London School of Medicine, Department of Haematological Medicine, Rayne Institute, King's College London School of Medicine, London, UK.
  • Padron E; King's College London School of Medicine, Department of Haematological Medicine, Rayne Institute, King's College London School of Medicine, London, UK.
Leukemia ; 30(3): 666-73, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26514544
Assuntos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Síndromes Mielodisplásicas / Leucemia Mieloide Aguda / Proteína Supressora de Tumor p53 / Frequência do Gene / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Leukemia Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Síndromes Mielodisplásicas / Leucemia Mieloide Aguda / Proteína Supressora de Tumor p53 / Frequência do Gene / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Leukemia Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos