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一个遗传性凝血因子XIII缺陷症家系的基因诊断
OBJECTIVE: To perform phenotypic diagnosis, genetic diagnosis and prenatal diagnosis of inherited coagulation factor XIII (FXIII) deficiency in a Chinese family also provide a review of inherited coagulation F XIII deficiency. METHODS: The activity levels of F XIII (F XIII:C) of proband and family m...
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| Vydáno v: | Zhonghua Xue Ye Xue Za Zhi |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Editorial office of Chinese Journal of Hematology
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7364940/ https://ncbi.nlm.nih.gov/pubmed/26477763 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.10.008 |
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