Integrated facial analysis and targeted sequencing identifies a novel KDM6A pathogenic variant resulting in Kabuki syndrome
Abstract. Kabuki syndrome (KS) is a rare congenital mental retardation condition characterized by facial dysmorphia, visceral and skeletal malformations, and developmental delay. The integrated phenotype and genotype-based prioritization is critical for diagnoses of genetic diseases. In this study,...
Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Health
2018-12-01
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Series: | Journal of Bio-X Research |
Online Access: | http://journals.lww.com/10.1097/JBR.0000000000000022 |