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
Trio‐WES reveals a novel de novo missense mutation of KMT2A in a Chinese patient with Wiedemann‐Steiner syndrome: A case report
Publication with shared reference
10.1002/mgg3.1533
Home
Publications
Trio‐WES reveals a novel de novo missense mutation of KMT2A in a Chinese patient with Wiedemann‐Steiner syndrome: A case report
Publication with shared reference
10.1002/mgg3.1533
Publications with shared reference:
Trio‐WES reveals a novel
de novo
missense mutation of
KMT2A
in a Chinese patient with Wiedemann‐Steiner syndrome: A case report
0
publications found
Export
Export
Analytics view
Analytics view
Scroll to top