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Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.
Casini, A; Brungs, T; Lavenu-Bombled, C; Vilar, R; Neerman-Arbez, M; de Moerloose, P.
Afiliação
  • Casini A; Division of Angiology and Haemostasis, Faculty of Medicine, University Hospitals of Geneva, Geneva, Switzerland.
  • Brungs T; Service d'Hématologie Biologique, Hôpital Bicêtre, Assistance Publique-Hôpitaux de Paris, Le Kremlin-Bicêtre, France.
  • Lavenu-Bombled C; Service d'Hématologie Biologique, Hôpital Bicêtre, Assistance Publique-Hôpitaux de Paris, Le Kremlin-Bicêtre, France.
  • Vilar R; Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
  • Neerman-Arbez M; Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
  • de Moerloose P; Division of Angiology and Haemostasis, Faculty of Medicine, University Hospitals of Geneva, Geneva, Switzerland.
J Thromb Haemost ; 15(5): 876-888, 2017 05.
Article em En | MEDLINE | ID: mdl-28211264
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coagulação Sanguínea / Fibrinogênio / Mutação de Sentido Incorreto / Afibrinogenemia Tipo de estudo: Diagnostic_studies / Prognostic_studies / Systematic_reviews Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coagulação Sanguínea / Fibrinogênio / Mutação de Sentido Incorreto / Afibrinogenemia Tipo de estudo: Diagnostic_studies / Prognostic_studies / Systematic_reviews Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article