Showing results 1 to 3 of 3
| Title | Author(s) | Issue Date | |
|---|---|---|---|
Clinical implications of large rare copy number variations in 110 Chinese patients with conotruncal heart disease Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014 | 2014 | ||
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients Journal:npj Genomic Medicine | 2016 | ||
Practical guidelines for managing adults with 22q11.2 deletion synddrome Journal:Genetics in Medicine | 2015 |