VIICTR
Profiles
ORIT
Pediatrics RRO
Home
About
Overview
Sharing Data
ORCID
Help
History (1)
Detection of clinically relevant copy number variants with whole-exome sequencing.
See All Pages
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
Detection of clinically relevant copy number variants with whole-exome sequencing.
Detection of clinically relevant copy number variants with whole-exome sequencing. Hum Mutat. 2013 Oct; 34(10):1439-48.
View in:
PubMed
subject areas
Algorithms
DNA Copy Number Variations
Exome
Genetic Testing
Genome-Wide Association Study
High-Throughput Nucleotide Sequencing
Humans
Intellectual Disability
Reproducibility of Results
authors with profiles
JAMES LUPSKI