Showing results 1 to 3 of 3
Title | Author(s) | Issue Date | |
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Clinical implications of large rare copy number variation in 110 Chinese patients with conotruncal heart disease Proceeding/Conference:ASPR-JPS 2015 Joint Meeting | 2015 | ||
Identifying genetic mutations in patients with rasopathies using a next generation sequencing diagnostic pipeline in Hong Kong Proceeding/Conference:ASPR-JPS 2015 Joint Meeting | 2015 | ||
Whole-exome sequencing identified CC2D1A as the candidate gene for right isomerism Proceeding/Conference:ASPR-JPS 2015 Joint Meeting | 2015 |