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Application of High-Throughput Sequencing in the Diagnosis of Inherited Thrombocytopenia
Inherited thrombocytopenia is a group of hereditary diseases with a reduction in platelet count as the main clinical manifestation. Clinically, there is an urgent need for a convenient and rapid diagnosis method. We introduced a high-throughput, next-generation sequencing (NGS) platform into the rou...
Tallennettuna:
| Julkaisussa: | Clin Appl Thromb Hemost |
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| Päätekijät: | , , , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
SAGE Publications
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6714838/ https://ncbi.nlm.nih.gov/pubmed/30103613 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1076029618790696 |
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