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[Clinical and Molecular Genetic Analysis of a Child with Comorbid 16p11.2 Microdeletion Syndrome and Rett Syndrome].

Pengwu Lin,Xuan Feng,Shengju Hao,Chunyang Jia, Hairui Pan,Chuan Zhang,Ling Hui, Qinghua Zhang

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics（2024）

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Key words
Chromosome,16p11.2 microdeletion syndrome,Rett syndrome,Whole exome sequencing,MECP2 gene
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