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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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| Publicado no: | Exp Ther Med |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2018
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| Assuntos: | |
| Acesso em linha: | 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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