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Utility of whole-genome sequencing in the clinical diagnostic of rare inherited anaemias

Utility of whole-genome sequencing in the clinical diagnostic of rare inherited anaemias

Bibliografiska uppgifter
Huvudupphovsmän: C Camps, NBA Roy, H Dreau, S Henderson, SJL Knight, EM Kvikstad, MM Pentony, M Proven, A Schuh, JC Taylor
Materialtyp: Conference item
Språk:English
Publicerad: Springer Nature 2018
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