Rankings
Publications
Search Publications
Cited-by Search
Sources
Publishers
Scholars
Scholars
Top Cited Scholars
Organizations
About
Scilit
About Us
Advisory Board
Data Sources
Career
Support / Contact
User Guide
Publisher User
Search Function
Rankings Function
API Resource
Scilit Knowledge
Metrics
Scilit Recognitions
Publications Classification
Media
News
Blog
Login
Register
Home
Publications
Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome
Publication with shared reference
10.1002/mgg3.70238
Home
Publications
Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome
Publication with shared reference
10.1002/mgg3.70238
Publications with shared reference:
Identification and Functional Analysis of a Novel
NSD2
Missense Variant in a Patient With Rauch‐Steindl Syndrome
0
publications found
Export
Export
Analytics view
Analytics view
Scroll to top