165 related articles for article (PubMed ID: 26037343)
1. [Congenital hypofibrinogenemia associated with a novel mutation in FGG gene].
Wang Y; Ding H; Hao X; Zhu L; Yang L; Jin Y; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):331-4. PubMed ID: 26037343
[TBL] [Abstract][Full Text] [Related]
2. [Analysis of a pedigree affected with congenital hypofibrinogenemia due to heterozygous Ser313Ile mutation of fibrinogen γ chain gene].
Zhu L; Zhao M; Cheng X; Yu D; Li X; Xu F; Wang J; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):179-183. PubMed ID: 29652987
[TBL] [Abstract][Full Text] [Related]
3. [Mutation analysis of a FGG gene causing hereditary abnormal fibrinogen].
Jiang L; Zhang Q; Xu W; Zhang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec; 35(6):812-814. PubMed ID: 30512152
[TBL] [Abstract][Full Text] [Related]
4. [Fibrinogen gamma-chain mutation, p.Ile171His, leads to hereditary hypofibrinogenemia].
Liu JX; Wang CJ; Dai JH; Zhang MX; Lyu B; Jiang B
Zhonghua Nei Ke Za Zhi; 2022 Feb; 61(2):172-176. PubMed ID: 35090252
[No Abstract] [Full Text] [Related]
5. [Analysis of a pedigree affected with congenital dysfibrinogenemia due to a novel Gly31Glu mutation of FGA gene].
Wang X; Yang X; Yang W; Shu K; Li F; Liu J; Zhang Z; Li S; Jiang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Sep; 36(9):901-904. PubMed ID: 31515786
[TBL] [Abstract][Full Text] [Related]
6. [A case of inherited afibrinogenemia caused by an IVS7-12A>G splice mutation of FGG gene].
Wang X; Yang X; Wang J; Shu K; Li F; Yang W; Ruan J; Wang S; Jiang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec; 37(12):1391-1394. PubMed ID: 33306830
[TBL] [Abstract][Full Text] [Related]
7. A novel fibrinogen mutation (γ Thr277Arg) causes hereditary hypofibrinogenemia in a Chinese family.
Zhu L; Wang M; Xie H; Jin Y; Yang L; Xu P
Blood Coagul Fibrinolysis; 2013 Sep; 24(6):642-4. PubMed ID: 23492915
[TBL] [Abstract][Full Text] [Related]
8. [Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene].
Zhang J; Zhao XJ; Wang ZY; Yu ZQ; Cao LJ; Ma ZN; Zhang J; Zhang W; Bai X; Ruan CG
Zhonghua Xue Ye Xue Za Zhi; 2013 Sep; 34(9):751-6. PubMed ID: 24103871
[TBL] [Abstract][Full Text] [Related]
9. [Genetic analysis of a Chinese pedigree affected with Congenital dysfibrinogenemia due to variant of FGG gene].
Shao X; Ma J; Wang Z; Sun M; Huang Z; Jiang Z; Liu X; Li S; Liu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Nov; 40(11):1324-1329. PubMed ID: 37906135
[TBL] [Abstract][Full Text] [Related]
10. Novel mutations (γTrp208Leu and γLys232Thr) leading to congenital hypofibrinogenemia in two unrelated Chinese families.
Zhu L; Wang Y; Zhao M; Hao X; Xie H; Xie Y; Wang M; Ding H
Blood Coagul Fibrinolysis; 2014 Dec; 25(8):894-7. PubMed ID: 24914742
[TBL] [Abstract][Full Text] [Related]
11. [Clinical and genetic analysis of 8 Chinese pedigrees with inherited dysfibrinogenemia].
Jiang M; Wang X; Shu K; Jiang W; Huang Y; Lin Y; Li S; Hu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Apr; 31(2):134-9. PubMed ID: 24711018
[TBL] [Abstract][Full Text] [Related]
12. [Congenital Fibrinogen Deficiency Caused by Novel FGG Gene Mutation].
Wang TT; Shao JR; Wang J; Cheng Y; Zhang XQ; Fang YH; Yao CF; Zhang XS
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2021 Apr; 29(2):586-590. PubMed ID: 33812435
[TBL] [Abstract][Full Text] [Related]
13. [Congenital afibrinogenemia associated with a novel nonsense mutation in the FGA gene].
Wu SY; Wang ZY; Dong NZ; Bai X; Ruan CG
Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):133-6. PubMed ID: 15946522
[TBL] [Abstract][Full Text] [Related]
14. Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia.
Fang Y; Dai BT; Wang XF; Fu QH; Dai J; Xie F; Cai XH; Wang HL; Wang ZY
Haemophilia; 2006 Nov; 12(6):615-20. PubMed ID: 17083511
[TBL] [Abstract][Full Text] [Related]
15. [A Family with Congenital Dysfibrinogenemia and Blood Transfusion].
Liao XC; Zhang SS; Yang ZJ; Zhu CL; Huang HN; Luo RX; Li SN; Xie HQ; Li HL; Mo ZN
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2023 Oct; 31(5):1469-1474. PubMed ID: 37846702
[TBL] [Abstract][Full Text] [Related]
16. [Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen].
Yan J; Deng D; Deng X; Luo M; Cheng P; Liao L; Lin F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):160-3. PubMed ID: 27060305
[TBL] [Abstract][Full Text] [Related]
17. [Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia].
Ouyang Q; Ding QL; Huang DD; Xu GQ; Zhang LW; Dai J; Lu YL; Wang XF; Xi XD; Wang HL
Zhonghua Xue Ye Xue Za Zhi; 2011 Mar; 32(3):153-7. PubMed ID: 21535951
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel splicing mutation in the fibrinogen gamma chain gene leading to dysfibrinogenaemia in a Chinese pedigree.
Huang D; Chen H; Hu X; Wang X; Wang H
Pathology; 2015 Feb; 47(2):145-50. PubMed ID: 25551304
[TBL] [Abstract][Full Text] [Related]
19. Combined Congenital Hypodysfibrinogemia and Factor XI Deficiency in a Chinese Family.
Peng Y; Nie L; Qin C; Wan L; Zhou P
Acta Haematol; 2020; 143(5):472-477. PubMed ID: 31982874
[TBL] [Abstract][Full Text] [Related]
20. [Inherited afibrinogenemia caused by compound heterozygous mutations in the beta beta-chain of fibrinogen].
Fang Y; Wang HL; Wang XF; Fu QH; Wang WB; Xie S; Zhou RF; Dai J; Wang ZY
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Dec; 13(6):1086-9. PubMed ID: 16403286
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]