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十例遗传性凝血因子Ⅺ缺陷症患者的临床特征与基因突变分析

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840561/
https://www.ncbi.nlm.nih.gov/pubmed/33445854
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.12.013
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spelling pubmed-78405612021-01-28 十例遗传性凝血因子Ⅺ缺陷症患者的临床特征与基因突变分析 Zhonghua Xue Ye Xue Za Zhi 短篇论著 Editorial office of Chinese Journal of Hematology 2020-12 /pmc/articles/PMC7840561/ /pubmed/33445854 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.12.013 Text en 2020年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 短篇论著
十例遗传性凝血因子Ⅺ缺陷症患者的临床特征与基因突变分析
title 十例遗传性凝血因子Ⅺ缺陷症患者的临床特征与基因突变分析
title_full 十例遗传性凝血因子Ⅺ缺陷症患者的临床特征与基因突变分析
title_fullStr 十例遗传性凝血因子Ⅺ缺陷症患者的临床特征与基因突变分析
title_full_unstemmed 十例遗传性凝血因子Ⅺ缺陷症患者的临床特征与基因突变分析
title_short 十例遗传性凝血因子Ⅺ缺陷症患者的临床特征与基因突变分析
title_sort 十例遗传性凝血因子ⅺ缺陷症患者的临床特征与基因突变分析
topic 短篇论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840561/
https://www.ncbi.nlm.nih.gov/pubmed/33445854
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.12.013
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