VIICTR Profiles
ORIT
Pediatrics CRA
Home
About
Overview
Sharing Data
ORCID
Help
History (0)
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
Search Results
BI, WEIMIN
One or more keywords matched the following items that are connected to
BI, WEIMIN
Item Type
Name
Academic Article
Neurodevelopmental and neurobehavioral characteristics in males and females with CDKL5 duplications.
Academic Article
Whole exome sequencing identifies the first STRADA point mutation in a patient with polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome (PMSE).
Concept
Megalencephaly
Academic Article
Clinical characterization of individuals with the distal 1q21.1 microdeletion.
Search Criteria
Megalencephaly