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Genetic testing in bleeding disorders
The aim of molecular genetic analysis in families with haemophilia is to identify the causative mutation in an affected male as this provides valuable information for the patient and his relatives. For the patient, mutation identification may highlight inhibitor development risk or discrepancy betwe...
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| 發表在: | Haemophilia |
|---|---|
| Main Authors: | , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2014
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4274362/ https://ncbi.nlm.nih.gov/pubmed/24762276 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/hae.12409 |
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