Information

R4

R4: Classic CdLS is usually caused by variants in NIPBL; however, variants in one of six other genes – SMC1A, SMC3, RAD21, BRD4, HDAC8 or ANKRD11/ – should also be considered, as they may lead to a similar phenotype.

Find other pages that share the same topic as this page Moleculair diagnostic criteria3
Page history
Last modified by Gerritjan Koekkoek on 2020/07/02 14:48
Created by Gerritjan Koekkoek on 2020/07/02 14:48
On this site

About the website contents

 

All of the information on this WebSite is for education purposes only. The place to get specific medical advice, diagnoses, and treatment is your doctor. Use of this site is strictly at your own risk. If you find something that you think needs correction or clarification, please let us know at: 

Send a email: info@rtsyndroom.nl