Utility of whole-genome sequencing in the clinical diagnostic of rare inherited anaemias
Main Authors: | , , , , , , , , , |
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Format: | Conference item |
Jezik: | English |
Izdano: |
Springer Nature
2018
|
Main Authors: | , , , , , , , , , |
---|---|
Format: | Conference item |
Jezik: | English |
Izdano: |
Springer Nature
2018
|