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HARVARD Citation
Martin, E. et al. (2020). Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice. Human molecular genetics. pp. 3662-3678. [Online].
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Martin, E. et al. (2020). Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice. Human molecular genetics. pp. 3662-3678. [Online].