Your browser doesn't support javascript.
loading
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
Broderick, Peter; Chubb, Daniel; Johnson, David C; Weinhold, Niels; Försti, Asta; Lloyd, Amy; Olver, Bianca; Ma, Yussanne; Dobbins, Sara E; Walker, Brian A; Davies, Faith E; Gregory, Walter A; Childs, J Anthony; Ross, Fiona M; Jackson, Graham H; Neben, Kai; Jauch, Anna; Hoffmann, Per; Mühleisen, Thomas W; Nöthen, Markus M; Moebus, Susanne; Tomlinson, Ian P; Goldschmidt, Hartmut; Hemminki, Kari; Morgan, Gareth J; Houlston, Richard S.
Afiliação
  • Broderick P; Molecular and Population Genetics, Division of Genetics and Epidemiology, Institute of Cancer Research, Surrey, UK.
  • Chubb D; Molecular and Population Genetics, Division of Genetics and Epidemiology, Institute of Cancer Research, Surrey, UK.
  • Johnson DC; Haemato-Oncology Research Unit, Division of Molecular Pathology, Institute of Cancer Research, Surrey, UK.
  • Weinhold N; Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany.
  • Försti A; German Cancer Research Center, Heidelberg, Germany.
  • Lloyd A; Molecular and Population Genetics, Division of Genetics and Epidemiology, Institute of Cancer Research, Surrey, UK.
  • Olver B; Molecular and Population Genetics, Division of Genetics and Epidemiology, Institute of Cancer Research, Surrey, UK.
  • Ma Y; Molecular and Population Genetics, Division of Genetics and Epidemiology, Institute of Cancer Research, Surrey, UK.
  • Dobbins SE; Molecular and Population Genetics, Division of Genetics and Epidemiology, Institute of Cancer Research, Surrey, UK.
  • Walker BA; Haemato-Oncology Research Unit, Division of Molecular Pathology, Institute of Cancer Research, Surrey, UK.
  • Davies FE; Haemato-Oncology Research Unit, Division of Molecular Pathology, Institute of Cancer Research, Surrey, UK.
  • Gregory WA; University of Leeds, Leeds, UK.
  • Childs JA; University of Leeds, Leeds, UK.
  • Ross FM; Cytogenetics Group, Wessex Regional Cytogenetic Laboratory, Salisbury, UK.
  • Jackson GH; Royal Victoria Infirmary, Newcastle-on-Tyne, UK.
  • Neben K; Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany.
  • Jauch A; Institute of Human Genetics, University of Heidelberg, Germany.
  • Hoffmann P; Institute of Human Genetics, University of Bonn, Germany.
  • Mühleisen TW; Institute of Human Genetics, University of Bonn, Germany.
  • Nöthen MM; Institute of Human Genetics, University of Bonn, Germany.
  • Moebus S; German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
  • Tomlinson IP; Institute for Medical Informatics, Biometry and Epidemiology, University Hospital Essen, University Duisburg-Essen, Germany.
  • Goldschmidt H; Molecular and Population Genetics, Wellcome Trust Centre for Human Genetics, Oxford, OX3 7BN, UK.
  • Hemminki K; Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany.
  • Morgan GJ; National Centre of Tumour Diseases, Heidelberg, Germany.
  • Houlston RS; German Cancer Research Center, Heidelberg, Germany.
Nat Genet ; 44(1): 58-61, 2011 Nov 27.
Article em En | MEDLINE | ID: mdl-22120009
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Cromossomos Humanos Par 3 / Cromossomos Humanos Par 7 / Mieloma Múltiplo Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2011 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Cromossomos Humanos Par 3 / Cromossomos Humanos Par 7 / Mieloma Múltiplo Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2011 Tipo de documento: Article País de afiliação: Reino Unido