Associated Papers
A novel ZIC3 gene mutation identified in patients with heterotaxy and congenital heart disease.
Li S et al.
Scientific Reports, 2018
Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.
Paulussen AD et al.
European Journal of Human Genetics : Ejhg, 2016
A systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this field.
El Malti R et al.
European Journal of Human Genetics : Ejhg, 2016
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