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
CHEUNG, SAU WAI
One or more keywords matched the following items that are connected to
CHEUNG, SAU WAI
Item Type
Name
Academic Article
De novo and complex imbalanced chromosomal rearrangements revealed by array CGH in a patient with an abnormal phenotype and apparently "balanced" paracentric inversion of 14(q21q23).
Academic Article
Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?
Academic Article
Severe mental retardation, seizures, and hypotonia due to deletions of MEF2C.
Academic Article
Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions.
Concept
Muscle Hypotonia
Academic Article
Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays.
Search Criteria
Muscle Hypotonia