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血友病B的基因诊断
引用本文:张媛,郭智,何学鹏.血友病B的基因诊断[J].国际遗传学杂志,2010,33(2):303-305,309.
作者姓名:张媛  郭智  何学鹏
作者单位:北京军区总医院血液科,100700;
摘    要:The haemophilia B(HB)is caused by the mutations in the factⅨ gene, and is known as an X-linked recessive disease. At present, due to lacking of the eradicative therapy, the gene diagnosis and detection of the carriers is an effective method to prevent the infant patients to be born, block the transmission of harmful gene, and improve the population quality. This should be actively encouraged for its pratical usefulness.

关 键 词:血友病B    基因诊断    

The gene diagnosis of haemophilia B
ZHANG Yuan,GUO Zhi,HE Xue-peng.The gene diagnosis of haemophilia B[J].International JOurnal of Genetics,2010,33(2):303-305,309.
Authors:ZHANG Yuan  GUO Zhi  HE Xue-peng
Abstract:
Keywords:Haemophilia BGene diagnosis
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