Showing results 2 to 3 of 3
< previous
Title | Author(s) | Issue Date | Views | |
---|---|---|---|---|
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients Journal:npj Genomic Medicine | 2016 | 82 | ||
Practical guidelines for managing adults with 22q11.2 deletion synddrome Journal:Genetics in Medicine | 2015 | 70 |