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

Bibliographic Details
Main Authors: Hua Zhang, Li-Ming Yang, Lu Yuan, Xin Tan, Fu-Qing Zhang
Format: Article
Language:English
Published: Wolters Kluwer 2018-01-01
Series:Chinese Medical Journal
Online Access:http://www.cmj.org/article.asp?issn=0366-6999;year=2018;volume=131;issue=19;spage=2384;epage=2385;aulast=Zhang
Description
ISSN:0366-6999

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