Jin YH - Search Results

1

[Analysis of an hereditary protein C deficiency pedigree with compound heterozygous gene mutations].

Yang LH, Zhu LQ, Yang XO, Wang MS, Li J, Chen BC, Jin YH, Zhang Z, Zheng FX. Yang LH, et al. Among authors: jin yh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Oct;29(5):515-8. doi: 10.3760/cma.j.issn.1003-9406.2012.05.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23042384 Chinese.

2

Trinucleotide expansions in the SCA7 gene in a large family with spinocerebellar ataxia and craniocervical dystonia.

Lin Y, Zheng JY, Jin YH, Xie YC, Jin ZB. Lin Y, et al. Among authors: jin zb, jin yh. Neurosci Lett. 2008 Mar 28;434(2):230-3. doi: 10.1016/j.neulet.2008.01.077. Epub 2008 Feb 13. Neurosci Lett. 2008. PMID: 18325672

3

Identification of compound heterozygous mutations in the ITGA2B gene in a Chinese patient with Glanzmann thrombasthenia.

Zheng JY, Jin YH, Zhu YL, Jin PP, Zhang DT, Jin ZB. Zheng JY, et al. Among authors: jin zb, jin pp, jin yh. Chin Med J (Engl). 2010 Jun;123(11):1397-401. Chin Med J (Engl). 2010. PMID: 20819594

4

[An inherited coagulation factor VII deficiency pedigree caused by homozygous mutation of His348Gln].

Jin YH, Wang MS, Niu ZZ, Xie YS, Xie HX, Yang LH. Jin YH, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Feb;28(1):10-3. doi: 10.3760/cma.j.issn.1003-9406.2011.01.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21287501 Chinese.

5

Congenital combined deficiency of factor VII and X in a patient due to accidental diphacinone intoxication.

Zheng F, Jin Y, Wang M, Niu Z, Xu P, Xie H. Zheng F, et al. Thromb Haemost. 2011 Jul;106(1):180-1. doi: 10.1160/TH10-11-0732. Epub 2011 May 5. Thromb Haemost. 2011. PMID: 21544315 No abstract available.

6

[Analysis of an hereditary coagulation factor XII deficiency in a consanguineous pedigree].

Zhang Y, Xie HX, Wang MS, Jin YH, Xie YS, Zheng FX. Zhang Y, et al. Among authors: jin yh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):666-9. doi: 10.3760/cma.j.issn.1003-9406.2011.06.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 22161101 Chinese.

7

[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. Wang MS, et al. Among authors: jin yh. Zhonghua Xue Ye Xue Za Zhi. 2011 Dec;32(12):854-7. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 22339961 Chinese.

8

[Molecular genetics and clinical features of nine patients with inherited coagulation factor VII deficiency].

Jin YH, Wang MS, Zheng FX, Xie YS, Xie HX, Xu PF. Jin YH, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):404-7. doi: 10.3760/cma.j.issn.1003-9406.2012.04.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875495 Chinese.

9

[Analysis of phenotype and genotype in a Chinese pedigree with inherited prothrombin deficiency resulted from a homozygous mutation Tyr510Asp].

Jin YH, Wang MS, Zheng FX. Jin YH, et al. Zhonghua Xue Ye Xue Za Zhi. 2012 Jul;33(7):587-9. Zhonghua Xue Ye Xue Za Zhi. 2012. PMID: 22967428 Chinese. No abstract available.

10

Double heterozygous mutations Gln100Leu and His348Gln of the F7 gene in a patient with factor VII deficiency.

Li M, Zheng F, Jin Y, Wang M, Zhu L, Yang L. Li M, et al. Blood Coagul Fibrinolysis. 2013 Mar;24(2):199-201. doi: 10.1097/MBC.0b013e3283551132. Blood Coagul Fibrinolysis. 2013. PMID: 23358202

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