169 related articles for article (PubMed ID: 30290666)
21. 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]
22. [Analysis of two pedigrees affected with inherited dysfibrinogenemia due to a novel c.1115 T>A variant of the FGB gene].
Wang X; Yao Y; Lin S; Wang J; Shu K; Ai X; Jiang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jun; 39(6):587-591. PubMed ID: 35773760
[TBL] [Abstract][Full Text] [Related]
23. Identification of a novel mutation in congenital afibrinogenemia in Iranian patients.
Nojehdeh ST; Mojbafan M; Masoodifard M; Amini M; Zeinali S
Blood Coagul Fibrinolysis; 2021 Jul; 32(5):323-327. PubMed ID: 33901106
[TBL] [Abstract][Full Text] [Related]
24. Combined congenital dysfibrinogenemia and factor VII deficiency from mutations in the FGB and F7 genes.
Woo HI; Park IA; Lee KO; Kim SH; Kim HJ
Blood Coagul Fibrinolysis; 2012 Jul; 23(5):355-8. PubMed ID: 22576285
[TBL] [Abstract][Full Text] [Related]
25. A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.
Luo S; Xu Q; Xie Y; Li X; Jin Y; Yang L; Liu S; Wang M
Blood Coagul Fibrinolysis; 2020 Dec; 31(8):569-574. PubMed ID: 32833807
[TBL] [Abstract][Full Text] [Related]
26. Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.
Hua B; Li K; Lee A; Poon MC; Zhao Y
Haemophilia; 2015 Nov; 21(6):846-51. PubMed ID: 25982359
[TBL] [Abstract][Full Text] [Related]
27. A novel fibrinogen variant: dysfibrinogenemia associated with γAsp185Asn substitution.
Zhou N; Xu P; Zhou M; Xu Y; Li P; Chen B; Ouyang J; Zhou R
J Thromb Thrombolysis; 2017 Jul; 44(1):139-144. PubMed ID: 28425010
[TBL] [Abstract][Full Text] [Related]
28. [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]
29. 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]
30. [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]
31. [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]
32. An
Mischke R; Metzger J; Distl O
Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356081
[TBL] [Abstract][Full Text] [Related]
33. [Pedigree Analysis and Diagnosis of Congenital Dysfibrinogenemia: A Case Report].
Luo J; Duan SR; Wang H
Sichuan Da Xue Xue Bao Yi Xue Ban; 2022 Jan; 53(1):171-174. PubMed ID: 35048620
[TBL] [Abstract][Full Text] [Related]
34. [Fibrinogen beta chain gene mutation contributes to one congenital afibrinogenemia].
Xu XC; Zhou RF; Wu JS; Fang Y; Wang XF; Zhai ZM; Wang HL
Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):137-9. PubMed ID: 15946523
[TBL] [Abstract][Full Text] [Related]
35. Congenital fibrinogen disorder caused by digenic mutations of the
Wang X; Tang N; Shen N; Lu Y; Li D
Hematology; 2020 Dec; 25(1):145-148. PubMed ID: 32228225
[No Abstract] [Full Text] [Related]
36. 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]
37. Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families.
Amri Y; Toumi Nel H; Hadj Fredj S; de Moerloose P
Thromb Res; 2016 Jul; 143():11-6. PubMed ID: 27164460
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.
Neerman-Arbez M; Vu D; Abu-Libdeh B; Bouchardy I; Morris MA
Blood; 2003 May; 101(9):3492-4. PubMed ID: 12511408
[TBL] [Abstract][Full Text] [Related]
40. Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population.
Shen MC; Wang JD; Tsai W; Lin CY; Lin JS; Kuo SF; Lin PT; Huang YC; Hung MH
Haemophilia; 2021 Nov; 27(6):1022-1027. PubMed ID: 34460979
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]