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先天性心脏病(CHD)是人类最常见的出生缺陷,虽然其具体的发病机制至今仍不完全清楚,但遗传和环境因素已被证实是其主要的病因。本文着重就近年CHD的分子遗传学研究进展进行了综述。
Congenital heart disease (CHD) is the most common birth defects in humans. Although its specific pathogenesis is still not fully understood, genetic and environmental factors have been identified as the major causes. This article focuses on recent advances in molecular genetics CHD reviewed.