共 17 条
- [1] A commentary on de novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux Journal of Human Genetics, 2016, 61 : 773 - 774
- [2] De novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux Journal of Human Genetics, 2016, 61 : 835 - 838