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α-thalassaemia combined with hereditary spherocytosis in the same patient

A family of four from the Guangxi Zhuang Autonomous Region of China, including a child with α-thalassaemia and hereditary spherocytosis (HS), underwent laboratory identification, and genetic analysis. After harvesting peripheral blood samples from the child patient and his family members, GAP-polyme...

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Foilsithe in:Exp Ther Med
Main Authors: Li, Xiaohong, Liao, Lin, Deng, Xuelian, Huang, Jian, Deng, Zengfu, Wei, Hongying, Mo, Wuning, Lin, Faquan
Formáid: Artigo
Teanga:Inglês
Foilsithe: D.A. Spandidos 2018
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5774485/
https://ncbi.nlm.nih.gov/pubmed/29434716
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2017.5579
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