☆
4.5
Article
Identification of single gene deletions at15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype
CLINICAL GENETICS (2013)
Rate this paper
The primary rating indicates the level of overall quality for the paper. Secondary ratings independently reflect strengths or weaknesses of the paper.
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started