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

Hua Zhang Li-Ming Yang LU Yuan Xin Tan Fu-Qing Zhang

中华医学杂志（英文版）2018，Vol.131Issue(19)：2384-2385,2.

中华医学杂志（英文版）2018，Vol.131Issue(19)：2384-2385,2.DOI:10.4103/0366-6999.241793

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

Hua Zhang ¹Li-Ming Yang ¹LU Yuan ¹Xin Tan ²Fu-Qing Zhang¹

作者信息

1. Department of Eugenics and Genetics, Women and Infants Hospital of Zhengzhou, Zhengzhou, Henan 45000, China
2. Department of Neonatology, Women and Infants Hospital of Zhengzhou, Zhengzhou, Henan 45000, China
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Hua Zhang,Li-Ming Yang,LU Yuan,Xin Tan,Fu-Qing Zhang..A New Mutation Identified by Whole Exome Sequencing in a Cornelia de Lange Syndrome Newborn[J].中华医学杂志（英文版）,2018,131(19):2384-2385,2.

中华医学杂志（英文版）

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ISSN：0366-6999

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