346 related articles for article (PubMed ID: 27264807)
1. [Homozygous missense mutation p.Val298Met of F10 gene causing hereditary coagulation factor X deficiency in a Chinese pedigree].
Jin Y; Hao X; Cheng X; Yang L; Chen Y; Xie H; Wang Y; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):296-9. PubMed ID: 27264807
[TBL] [Abstract][Full Text] [Related]
2. [Phenotype and genotype analysis for a consanguineous pedigree with combined coagulation factor VII and X deficiency].
Jin Y; Wang M; Wang Y; Yang X; Yang L; Xie Y; Xie H; Zhu L; Yu F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):16-20. PubMed ID: 24510554
[TBL] [Abstract][Full Text] [Related]
3. [Genotypic and phenotypic analysis of a case with inherited coagulation factor X deficiency].
Chen T; Li F; Shu K; Liu J; Shen C; Zhang Z; Jin S; Wang X; Jiang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):544-547. PubMed ID: 30098253
[TBL] [Abstract][Full Text] [Related]
4. [Gene analysis of a combined inherited factor VII and factor X deficiency pedigree].
Wang MS; Jin YH; Zheng FX; Xie HX; Xu PF; Niu ZZ
Zhonghua Xue Ye Xue Za Zhi; 2011 Dec; 32(12):854-7. PubMed ID: 22339961
[TBL] [Abstract][Full Text] [Related]
5. [Analysis of a consanguineous pedigree featuring hereditary coagulation factor Ⅴ deficiency].
Xie YS; Zhang Y; Zhu LQ; Jin YH; Yang LH; Xie HX; Wang MS; Yang XL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):161-4. PubMed ID: 23568726
[TBL] [Abstract][Full Text] [Related]
6. Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X.
Chafa O; Tagzirt M; Tapon-Bretaudière J; Reghis A; Fischer AM; LeBonniec BF
Thromb Res; 2009 May; 124(1):144-8. PubMed ID: 19135706
[TBL] [Abstract][Full Text] [Related]
7. [Inherited coagulation factor X deficiency caused by two novel mutations in factor X gene].
Wang WB; Wang HL; Wang XF; Fu QH; Zhou RF; Xie S; Hu YQ; Wang ZY
Zhonghua Xue Ye Xue Za Zhi; 2004 Sep; 25(9):519-22. PubMed ID: 15569527
[TBL] [Abstract][Full Text] [Related]
8. [Analysis of a consanguineous pedigree affected with hereditary coagulation factor XII deficiency caused by homozygous Gly341Arg mutation].
Yang L; Jin S; Ji W; Cheng X; Li X; Jin Y; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):69-73. PubMed ID: 29419864
[TBL] [Abstract][Full Text] [Related]
9. A Compound Heterozygosis of Two Novel Mutations Causes Factor X Deficiency in a Chinese Pedigree.
Lu S; Lin W; Ji H; Su M; Zhao X; Wang C
Acta Haematol; 2021; 144(2):176-181. PubMed ID: 32599596
[TBL] [Abstract][Full Text] [Related]
10. Diagnostic Error of a Patient with Combined Inherited Factor VII and Factor X Deficiency due to Accidental Ingestion of a Diphacinone Rodenticide.
Li M; Jin Y; Wang M; Xie Y; Ding H
Clin Lab; 2016 Nov; 62(11):2253-2256. PubMed ID: 28164683
[TBL] [Abstract][Full Text] [Related]
11. Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly.
Al-Hilali A; Wulff K; Abdel-Razeq H; Saud KA; Al-Gaili F; Herrmann FH
Thromb Haemost; 2007 Apr; 97(4):542-5. PubMed ID: 17393015
[TBL] [Abstract][Full Text] [Related]
12. [Analysis of an hereditary coagulation factor XII deficiency in a consanguineous pedigree].
Zhang Y; Xie HX; Wang MS; Jin YH; Xie YS; Zheng FX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):666-9. PubMed ID: 22161101
[TBL] [Abstract][Full Text] [Related]
13. A new factor X defect (factor X Padua 3): a compound heterozygous between true deficiency (Gly(380)-->Arg) and an abnormality (Ser(334)-->Pro).
Vianello F; Lombardi AM; Boldrin C; Luni S; Girolami A
Thromb Res; 2001 Nov; 104(4):257-64. PubMed ID: 11728527
[TBL] [Abstract][Full Text] [Related]
14. [Identification of a novel heterozygous mutation in a pedigree with hereditary coagulation factor XII deficiency].
Yang L; Hao X; Wang Y; Xie H; Jin Y; Zhu L; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):343-7. PubMed ID: 26037346
[TBL] [Abstract][Full Text] [Related]
15. [Analysis of a hereditary protein C deficient consanguineous pedigree caused by Phe139Val homozygous mutation].
Yang LH; Zhu LQ; Wang YY; Xie HX; Xie YS; Jin YH; Wang MS; Chen BC; Yang XL
Zhonghua Xue Ye Xue Za Zhi; 2013 Sep; 34(9):767-70. PubMed ID: 24103874
[TBL] [Abstract][Full Text] [Related]
16. [Analysis on the novel compound heterozygous mutation FⅪ of a patient with hereditary factor Ⅺ deficiency].
Xu K; Shu KY; Li FF; Chen T; Liu J; Jin SS; Guo JJ; Zhang ZH; Jiang MH
Zhonghua Yi Xue Za Zhi; 2017 Dec; 97(48):3774-3778. PubMed ID: 29325334
[No Abstract] [Full Text] [Related]
17. [Genetic analysis of a pedigree with hereditary coagulation factor Ⅶ deficiency].
Jin Y; Wang Y; Hao X; Yang L; Xie H; Zhu L; Yu F; Yang X; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):222-5. PubMed ID: 25863091
[TBL] [Abstract][Full Text] [Related]
18. Severe factor X deficiency in three unrelated Palestinian patients is caused by homozygosity for the mutation c302delG-correlation with thrombin generation and thromboelastometry.
Livnat T; Shenkman B; Kenet G; Tamarin I; Gillis S; Varon D; Iijima K; Zivelin A; Salomon O
Blood Coagul Fibrinolysis; 2011 Dec; 22(8):673-9. PubMed ID: 22008904
[TBL] [Abstract][Full Text] [Related]
19. Impaired prothrombinase activity of factor X Gly381Asp results in severe familial CRM+ FX deficiency.
Pinotti M; Camire RM; Baroni M; Rajab A; Marchetti G; Bernardi F
Thromb Haemost; 2003 Feb; 89(2):243-8. PubMed ID: 12574802
[TBL] [Abstract][Full Text] [Related]
20. [Severe hereditary coagulation factor V deficiency caused by two novel heterozygous mutations].
Zhou RF; Fu QH; Xu XC; Wang WB; Wu WM; Ding QL; Xie S; Zhai ZM; Hu YQ; Wang XF; Wu JS; Wang HL
Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):129-32. PubMed ID: 15946520
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
