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MeSH:(Fibrinogens, Abnormal)

1.Mutation analysis of a FGG gene causing hereditary abnormal fibrinogen.

Liya JIANG ; Qiaohong ZHANG ; Wanping XU ; Yongjun ZHANG

Chinese Journal of Medical Genetics 2018;35(6):812-814

2.Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain.

Jing-yi ZHOU ; Xue-feng WANG ; Qiu-lan DING ; Guan-qun XU ; Li-wei ZHANG ; Jing DAI ; Ye-ling LU ; Xiao-dong XI ; Hong-li WANG

Chinese Journal of Hematology 2013;34(3):190-194

3.Fibrinogen Yecheon: Congenital Dysfibrinogenemia with Gamma Methionine-310 to Threonine Substitution.

Eunkyung PARK ; Geumbore PARK ; Rojin PARK ; Hee Jin KIM ; Sang Jae LEE ; Young Joo CHA

Journal of Korean Medical Science 2009;24(6):1203-1206

4.Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain.

Lin-lin JIANG ; Xue-feng WANG ; Qiu-lan DING ; Guan-qun XU ; Li-wei ZHANG ; Jing DAI ; Ye-ling LU ; Xiao-dong XI ; Hong-li WANG

Chinese Journal of Hematology 2012;33(6):475-479

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