| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8476144 | Mechanisms of Development | 2012 | 23 Pages |
Abstract
⺠22q11 hemizygosity: aberrant right subclavian artery and interrupted aortic arch type B. ⺠One change in the regulation of Ciona Ets1/2 is sufficient to convert a unicameral heart to a bicameral one. ⺠A sharp spatial gradient of Tbx5 is necessary and sufficient to septate the ventricle. ⺠Cilia mutations cause both heterotaxy and situs inversus totalis. ⺠Ciliary dysfunction affects the outcome of congenital heart disease in patients with heterotaxy.
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Authors
Alvin J. Chin, Jean-Pierre Saint-Jeannet, Cecilia W. Lo,