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
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders.
Academic Article
Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay.
Academic Article
Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions.
Concept
Child Development Disorders, Pervasive
Academic Article
Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics era.
Search Criteria
Child Development