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The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper
| Autores principales: | , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Lippincott Williams & Wilkins
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170004/ https://www.ncbi.nlm.nih.gov/pubmed/35686139 http://dx.doi.org/10.1097/HS9.0000000000000739 |
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| author | 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 |
| author_facet | 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 |
| author_sort | Roy, Noémi B. A. |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-9170004 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2022 |
| publisher | Lippincott Williams & Wilkins |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-91700042022-06-08 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 Hemasphere Guideline Article—Consensus based Lippincott Williams & Wilkins 2022-06-06 /pmc/articles/PMC9170004/ /pubmed/35686139 http://dx.doi.org/10.1097/HS9.0000000000000739 Text en Copyright © 2022 The Authors. On behalf of BSH and EHA. Published by John Wiley & Sons Limited/Wolters Kluwer (respectively). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CC-BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in anyway or used commercially without permission from the publisher. |
| spellingShingle | Guideline Article—Consensus based 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 The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper |
| title | The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper |
| title_full | The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper |
| title_fullStr | The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper |
| title_full_unstemmed | The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper |
| title_short | The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper |
| title_sort | use of next-generation sequencing in the diagnosis of rare inherited anaemias: a joint bsh/eha good practice paper |
| topic | Guideline Article—Consensus based |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170004/ https://www.ncbi.nlm.nih.gov/pubmed/35686139 http://dx.doi.org/10.1097/HS9.0000000000000739 |
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