Neonatal hereditary spherocytosis caused by a de novo frameshift mutation of the SPTB gene characterized by hydrops fetalis: A case report

por Zhang, Yimin, Shao, Shuming, Liu, Jie, Zeng, Chaomei, Han, Ye, Zhang, Xiaorui
Publicado 2021

Correlation between apelin and VEGF levels in retinopathy of prematurity: a matched case–control study

por Zhang, Yimin, Feng, Jing, Shao, Shuming, Mu, Qing, Liu, Jie, Zeng, Chaomei, Zhang, Xiaorui
Publicado 2022