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

Zhang, Hua

A New Mutation Identified by Whole Exome Sequencing in a Cornelia de Lange Syndrome Newborn. [electronic resource] - Chinese medical journal 10 2018 - 2384-2385 p. digital

Publication Type: Case Reports; Letter

2542-5641

10.4103/0366-6999.241793 doi


De Lange Syndrome--genetics
Female
Humans
Infant, Newborn
Mutation--genetics
Pedigree
Exome Sequencing--methods