A New Mutation Identified by Whole Exome Sequencing in a Cornelia de Lange Syndrome Newborn
oleh: Hua Zhang, Li-Ming Yang, Lu Yuan, Xin Tan, Fu-Qing Zhang
| Format: | Article |
|---|---|
| Diterbitkan: | Wolters Kluwer 2018-01-01 |
Deskripsi
No description available for this item.