Cite
HARVARD Citation
Miguet, M. et al. (2016). Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features. Prenatal diagnosis. pp. 1276-1279. [Online].
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Miguet, M. et al. (2016). Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features. Prenatal diagnosis. pp. 1276-1279. [Online].