Cite
HARVARD Citation
Alby, C. et al. (2018). Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomalies. American journal of medical genetics. 176 (5), pp. 1091-1098. [Online].
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Alby, C. et al. (2018). Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomalies. American journal of medical genetics. 176 (5), pp. 1091-1098. [Online].