Li T - Search Results

1

[Genetic analysis of a pedigree affected with distal hereditary motor neuronopathy V].

Li T, Lyu X, Xiao H, Li L, Guo Q, Wang H, Zhang B, Zhang C, Wang X, Liao S. Li T, et al. Among authors: li l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):207-211. doi: 10.3760/cma.j.issn.1003-9406.2019.03.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30835347 Chinese.

2

[Association of MTHFR and MTRR genes polymorphisms with non-disjunctions of chromosomes 18 and 21].

Guo Q, Wang H, Yang K, Zhang B, Li T, Liao S. Guo Q, et al. Among authors: li t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Jun;32(3):395-9. doi: 10.3760/cma.j.issn.1003-9406.2015.03.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26037359 Chinese.

3

[Mutation analysis for a large Chinese family affected with MYH9-related thrombocytopenia].

Liu H, Li T, Wang H, Guo L, Wu D, Xiao H, Guo Q, Wang T. Liu H, et al. Among authors: li t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Oct;33(5):629-32. doi: 10.3760/cma.j.issn.1003-9406.2016.05.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27577209 Chinese.

4

[Analysis of genetic polymorphisms and mutations of 20 frequently used STR loci among ethnic Hans from Henan].

Wang H, Kang B, Gao Y, Huo X, Li T, Guo Q, Zhu B, Liao S. Wang H, et al. Among authors: li t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):266-269. doi: 10.3760/cma.j.issn.1003-9406.2017.02.026. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397234 Chinese.

5

[Phenotypic and genetic analysis of a boy with partial trisomy of 1q].

Wu D, Zhang H, Wang H, Hou Q, Wang T, Li T, Yang Y, Liao S. Wu D, et al. Among authors: li t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):398-401. doi: 10.3760/cma.j.issn.1003-9406.2017.03.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28604964 Chinese.

6

[Genetic and prenatal diagnosis for a haemophilia A family with two novel mutations of F8 gene].

Li T, Hou Q, Liu H, Xiao H, Zhang B, Liu S, Yang Y, Zhang C, Ding X, Liao S. Li T, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):486-489. doi: 10.3760/cma.j.issn.1003-9406.2017.04.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777843 Chinese.

7

[Prenatal diagnosis and genetic analysis of a fetus with 6q27 microdeletion].

Wu D, Shi W, Wang H, Hou Q, Zhang H, Li T, Zhang C, Yang Y, Liao S. Wu D, et al. Among authors: li t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Oct 10;34(5):718-721. doi: 10.3760/cma.j.issn.1003-9406.2017.05.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28981941 Chinese.

8

[Clinical and genetic analysis of a boy with 9q34.3 microdeletion syndrome].

Wu D, Li T, Wang H, Shi W, Hou Q, Zhang H, Wang T, Yang Y, Liao S. Wu D, et al. Among authors: li t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):849-852. doi: 10.3760/cma.j.issn.1003-9406.2017.06.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188614 Chinese.

9

[Analysis of pathological mutation in a Chinese pedigree affected with familial exudative vitreoretinopathy].

Su N, Qin L, Wang H, Xiao H, Guo Q, Li T, Liao S. Su N, et al. Among authors: li t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):193-196. doi: 10.3760/cma.j.issn.1003-9406.2018.02.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29652990 Chinese.

10

[Genetic analysis of a child with cleidocranial dysplasia and 6q21-q22.31 microdeletion].

Wu D, Li T, Hou Q, Huo X, Wang X, Wang T, Yang Y, Liu H, Liao S. Wu D, et al. Among authors: li t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):253-256. doi: 10.3760/cma.j.issn.1003-9406.2018.02.024. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29653004 Chinese.

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