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The use of next-generation sequencing in the diagnosis of r..:
Roy, Noémi B. A
;
Da Costa, Lydie
;
Russo, Roberta
...
British Journal of Haematology. , 2022
Link:
https://hdl.handle.net/20.500.12328/3410
RT Journal T1
The use of next-generation sequencing in the diagnosis of rare inherited anaemias: a joint BSH/EHA good practice paper
UL https://suche.suub.uni-bremen.de/peid=base-ftunivicatalunya:oai:repositori.uic.es:20.500.12328_3410&Exemplar=1&LAN=DE A1 Roy, Noémi B. A A1 Da Costa, Lydie A1 Russo, Roberta A1 Bianchi, Paola A1 Mañú-Pereira, Maria del Mar A1 Fermo, Elisa A1 Andolfo, Immacolata A1 Clark, Barnaby A1 Proven, Melanie A1 Sanchez-Fernandez, Mayka A1 Van Wijk, Richard A1 Van der Zwaag, Bert A1 Layton, Mark A1 Rees, David A1 Iolascon, Achille A1 British Society for Haematology/ European Hematology Association PB John Wiley & Sons YR 2022 K1 Anemia K1 Bones pràctiques K1 Atenció al pacient K1 Buenas prácticas K1 Atención al paciente K1 Good practices K1 Patient care K1 61 JF British Journal of Haematology LK http://dx.doi.org/https://hdl.handle.net/20.500.12328/3410 DO https://hdl.handle.net/20.500.12328/3410 SF ELIB - SuUB Bremen
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