Cite
HARVARD Citation
Boissel, S. et al. (2018). Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis. Genetics in medicine. pp. 745-753. [Online].
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Boissel, S. et al. (2018). Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis. Genetics in medicine. pp. 745-753. [Online].