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The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper.
Roy, Noémi B A; Da Costa, Lydie; Russo, Roberta; Bianchi, Paola; Del Mar Mañú-Pereira, Maria; Fermo, Elisa; Andolfo, Immacolata; Clark, Barnaby; Proven, Melanie; Sanchez, Mayka; van Wijk, Richard; van der Zwaag, Bert; Layton, Mark; Rees, David; Iolascon, Achille.
Afiliação
  • Roy NBA; Department of Haematology, Oxford University Hospitals, NHS Foundation Trust, Oxford, United Kingdom.
  • Da Costa L; NIHR BRC Blood Theme, Oxford, United Kingdom.
  • Russo R; Hôpital Universitaire Robert Debré, Paris, France.
  • Bianchi P; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Naples, Italy.
  • Del Mar Mañú-Pereira M; CEINGE Biotecnologie Avanzate, Naples, Italy.
  • Fermo E; UOS Fisiopatologia delle Anemie, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Milano, Italy.
  • Andolfo I; Translational research in Rare Anaemia Disorders, Vall d'Hebron Research Institute, Barcelona, Spain.
  • Clark B; UOS Fisiopatologia delle Anemie, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Milano, Italy.
  • Proven M; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Naples, Italy.
  • Sanchez M; CEINGE Biotecnologie Avanzate, Naples, Italy.
  • van Wijk R; King's College Hospital, King's College, London, United Kingdom.
  • van der Zwaag B; Genetics Laboratories, Oxford University Hospitals, NHS Foundation Trust, Oxford, United Kingdom.
  • Layton M; Department of Basic Sciences, Iron metabolism: Regulation and Diseases, Universitat Internacional de Catalunya (UIC), Barcelona, Spain.
  • Rees D; BloodGenetics S. L. Diagnostics in Inherited Blood Diseases, Barcelona, Spain.
  • Iolascon A; Central Diagnostic Laboratory, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Hemasphere ; 6(6): e739, 2022 Jun.
Article em En | MEDLINE | ID: mdl-35686139

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article