Cite
HARVARD Citation
Jones, G. et al. (2014). A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death. Journal of clinical pathology. 67 (3), pp. 283-284. [Online].
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Jones, G. et al. (2014). A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death. Journal of clinical pathology. 67 (3), pp. 283-284. [Online].