| 标题 |
Compound Heterozygosity for Null Mutations and a Common Hypomorphic Risk Haplotype in TBX6 Causes Congenital Scoliosis |
| 网址 | |
| DOI | |
| 其它 |
期刊:Human Mutation 作者:K. Takeda; I. Kou; N. Kawakami; A. Iida; M. Nakajima; et al 出版日期:2017-03-01 |
| 求助人 | |
| 下载 |
PDF的下载单位、IP信息已删除
(2025-6-4)