Cite
HARVARD Citation
Chérot, E. et al. (2018). Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients. Clinical genetics. 93 (3), pp. 567-576. [Online].
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Chérot, E. et al. (2018). Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients. Clinical genetics. 93 (3), pp. 567-576. [Online].