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The implication of 'unknown significance' variants in next-generation sequencing in diagnosis and donor selection for allogenic haematopoietic stem cell transplantation. Report of a case of myelodysplastic syndrome with a polymorphism in the tyrosin

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Description scientific article published on 08 April 2020
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author: Bernardo López-Andrade  Leyre Bento  María Díez-Campelo 

Publication date April 8, 2020
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