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Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies
Ma, Lijiang, Selamet Tierney, Elif Seda, Lee, Teresa, Lanzano, Patricia, Chung, Wendy K.Volume:
22
Language:
english
Journal:
Cardiology in the Young
DOI:
10.1017/S1047951111001181
Date:
April, 2012
File:
PDF, 860 KB
english, 2012