Cite
HARVARD Citation
Bick, D. et al. (2019). Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases. Journal of medical genetics. 56 (12), pp. 783-791. [Online].
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Bick, D. et al. (2019). Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases. Journal of medical genetics. 56 (12), pp. 783-791. [Online].