Cite
HARVARD Citation
Clement, E. et al. (2018). Hypochondroplasia and epilepsy: temporal lobe dysgenesis in FGFR3 mutations. Journal of the International Child Neurology Association. p. . [Online].
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Clement, E. et al. (2018). Hypochondroplasia and epilepsy: temporal lobe dysgenesis in FGFR3 mutations. Journal of the International Child Neurology Association. p. . [Online].