[对两家患有短肋胸部发育不良3型的家族进行基因分析]

Xin Guan1, Huan Mi, Shan Li

  • 1Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Department of Medical Genetics, School of Basic Medicine, Peking Union Medical College, Beijing 100005, China. xiulizhao@ibms.pumc.edu.cn.

概括

基因分析确定了DYNC2H1基因中的复合异合体变异,可能导致两个胎儿的带有或没有多节性肋骨 (SRTD3) 的短肋骨胸部形. 这一发现有助于理解SRTD病原体.

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