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Number of items: 1.

McBride, David J., Fielding, Claire, Newington, Taksina, Vatsiou, Alexandra, Fischl, Harry, Bajracharya, Maya, Thomson, Vicki S., Fraser, Louise J., Fujita, Pauline A., Becq, Jennifer, Kingsbury, Zoya, Ross, Mark T., Moat, Stuart J. and Morgan, Sian 2023. Whole-genome sequencing can identify clinically relevant variants from a single sub-punch of a dried blood spot specimen. International Journal of Neonatal Screening 9 (3) , 52. 10.3390/ijns9030052
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This list was generated on Tue Apr 30 06:58:37 2024 BST.