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

Detalles Bibliográficos
Autores principales:	C Camps, NBA Roy, H Dreau, S Henderson, SJL Knight, EM Kvikstad, MM Pentony, M Proven, A Schuh, JC Taylor
Formato:	Conference item
Lenguaje:	English
Publicado:	Springer Nature 2018

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