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HARVARD Citation
Pitsava, G. et al. (2022). Exome sequencing identifies variants in infants with sacral agenesis. Birth defects research. 114 (7), pp. 215-227. [Online].
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Pitsava, G. et al. (2022). Exome sequencing identifies variants in infants with sacral agenesis. Birth defects research. 114 (7), pp. 215-227. [Online].