Novel <i>SMAD3</i> Mutation in a Patient with Hypoplastic Left Heart Syndrome with Significant Aortic Aneurysm

<div class="floats-full-page floats-full-page-figure"><h2>Figure 1</h2><div class="floats-full-page-caption"><table>Optiray contrast-enhanced computed tomography images of the chest with sagittal (a) and coronal (b) reconstructions in the 14-year-old proband revealing aneurysmal dilation of the ascending aorta.</table></div><div class="floats-full-page-content"><table class="table-group" width="800px"><tr class="fig-image" id="a"><td><img alt="591516.fig.001a" src="https://static-01.hindawi.com/articles/crig/volume-2014/591516/figures/591516.fig.001a.jpg" /></td></tr><tr class="fig-caption"><td align="center"><table><tr><td><b>(a) </b></td></tr></table></td></tr><tr class="fig-image" id="b"><td><img alt="591516.fig.001b" src="https://static-01.hindawi.com/articles/crig/volume-2014/591516/figures/591516.fig.001b.jpg" /></td></tr><tr class="fig-caption"><td align="center"><table><tr><td><b>(b) </b></td></tr></table></td></tr></table></div></div>

Figure 1 | Novel <i>SMAD3</i> Mutation in a Patient with Hypoplastic Left Heart Syndrome with Significant Aortic Aneurysm

title

Figure 1: Novel <i>SMAD3</i> Mutation in a Patient with Hypoplastic Left Heart Syndrome with Significant Aortic Aneurysm

description

Figure 1 | Novel SMAD3 Mutation in a Patient with Hypoplastic Left Heart Syndrome with Significant Aortic Aneurysm

Figure 1

About this journal

<p><em>Case Reports in Genetics</em> publishes case reports and case series focusing on diseases caused by hereditary predisposition or genetic variation in individuals and families.</p>


Journal profile

Meet the editorial board

<p><em>Case Reports in Genetics</em> maintains an Editorial Board of practicing researchers from around the world, to ensure manuscripts are handled by editors who are experts in the field of study.</p>


Editor spotlight

Find out more

This journal's articles appear in a wide range of abstracting and indexing databases, and are covered by numerous other services that aid discovery and access. Find out more about where and how the content of this journal is available.