方法：在有左室发育不全和二叶式主动脉瓣先证者的家系中进行非参数基因组连锁分析。
Methods: Family - based nonparametric genome - wide linkage analysis was performed in by either an HLHS or BAV proband.
目的：研究少汗性外胚叶发育不全引起先天缺牙的ED1基因突变。
Objective: To detect ED1 gene mutation in three hypohidrotic ectodermal dysplasia (HED) nuclear families.
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