| Multiplex targeted high-throughput sequencing for Mendelian cardiac disorders | Clinical genetics |  | | 2014 | 751 | 0 |
|
| Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice | Journal of medical genetics |  | | 2011 | 678 | 0 |
|
| A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy | Human mutation |  | | 2008 | 760 | 0 |
|
| Candidate gene analysis in three families with acilia syndrome | American journal of medical genetics. Part A |  | | 2008 | 634 | 0 |
|
| DNAI1 mutations explain only 2% of primary ciliary dykinesia | Respiration |  | | 2008 | 834 | 510 |
|