Cite
HARVARD Citation
Evans, C. et al. (2019). Fetal diagnosis of Mowat‐Wilson syndrome by whole exome sequencing. American journal of medical genetics. 179 (10), pp. 2152-2157. [Online].
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Evans, C. et al. (2019). Fetal diagnosis of Mowat‐Wilson syndrome by whole exome sequencing. American journal of medical genetics. 179 (10), pp. 2152-2157. [Online].