The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper
Date
2022-08Permanent link
https://hdl.handle.net/11351/8102DOI
10.1111/bjh.18191
ISSN
2572-9241
PMID
35661144
DL
000805480600001
Keywords
Next-generation sequencing; Rare anemiaBibliographic citation
Roy NBA, Da Costa L, Russo R, Bianchi P, Mañú-Pereira MDM, Fermo E, et al. The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper*. Br J Haematol. 2022 Aug;198(3):459–77.
Audience
Professionals
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- VHIR - Articles científics [1751]
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