Cargando…
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...
Formato: | Online Artículo Texto |
---|---|
Lenguaje: | English |
Publicado: |
Editorial office of Chinese Journal of Hematology
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364940/ https://www.ncbi.nlm.nih.gov/pubmed/26477763 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.10.008 |