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5. A New Mutation Identified by Whole Exome Sequencing in a Cornelia de Lange Syndrome Newborn

A New Mutation Identified by Whole Exome Sequencing in a Cornelia de Lange Syndrome Newborn

来源 :中华医学杂志英文版 | 被引量 : 0次 | 上传用户：charles8025

【作 者】

：

ZhangHua YangLi-Ming YuanLu TanXin ZhangFu-Qing 

【机 构】

：

DepartmentofEugenicsandGenetics,WomenandInfantsHospitalofZhengzhou,Zhengzhou,Henan45000,China,Depart

【出 处】

：

中华医学杂志英文版

【发表日期】

：

2018年131期

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