| index | Title |
| 1 | A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect Author(s):Ji-jia Liu, Liang-liang Fan, Jin-lan Chen, Zhi-ping Tan, Yi-feng Yang Clicked:10388 Download:5157 Cited:8 <Full Text> <PPT> 3101 Journal of Zhejiang University Science B 2014 Vol.15 No.9 P.830-837 DOI:10.1631/jzus.B1400062 |
