![](/img/cover-not-exists.png)
Prenatal diagnosis of a rare β âthalassemia gene ï¼90 (C>T) ( HBB : c.â140 C>T) mutation associated with deletional Hb H disease (ââ SEA /â α 4.2 )
Qian, Hou, Huang, Jianlin, Xu, Ji, Zhao, Weihua, Ye, Xiufeng, Liu, WenlanJournal:
Molecular Genetics & Genomic Medicine
DOI:
10.1002/mgg3.1472
Date:
September, 2020
File:
PDF, 701 KB
2020