AM
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Multiplex targeted high-throughput sequencing for Mendelian cardiac disorders | Clinical genetics |  | 2014 | 744 | 0 | ||
| Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice | Journal of medical genetics | | 2011 | 673 | 0 | ||
| A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy | Human mutation | | 2008 | 756 | 0 | ||
| Candidate gene analysis in three families with acilia syndrome | American journal of medical genetics. Part A | | 2008 | 628 | 0 | ||
| DNAI1 mutations explain only 2% of primary ciliary dykinesia | Respiration | | 2008 | 827 | 510 |
