Li T - Search Results

1

A novel MIP mutation in familial congenital nuclear cataracts.

Qin L, Guo L, Wang H, Li T, Lou G, Guo Q, Hou Q, Liu H, Liao S, Liu Z. Qin L, et al. Among authors: li t. Eur J Med Genet. 2016 Sep;59(9):488-91. doi: 10.1016/j.ejmg.2016.07.002. Epub 2016 Jul 22. Eur J Med Genet. 2016. PMID: 27456987

2

[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.

3

[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.

4

Novel heterozygous mutations of the INSR gene in a familial case of Donohue syndrome.

Qin L, Li X, Hou Q, Wang H, Lou G, Li T, Wang L, Liu H, Li X, Liao S. Qin L, et al. Among authors: li t, li x. Clin Chim Acta. 2017 Oct;473:26-31. doi: 10.1016/j.cca.2017.08.007. Epub 2017 Aug 10. Clin Chim Acta. 2017. PMID: 28803747

5

[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.

6

[Analysis of ELN gene mutation in a pedigree affected with cutis laxa].

Xiao H, Zhang Z, Lyu X, Li T, Guo Q, Wang H, Zhang Q, Su J, Liao S. Xiao H, et al. Among authors: li t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Aug 10;36(8):785-788. doi: 10.3760/cma.j.issn.1003-9406.2019.08.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31400128 Chinese.

7

[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.

8

Diagnosis with Multiple Epiphyseal Dysplasia Using Whole-exome Sequencing in a Chinese Family.

Liu HY, Xiao JF, Huang J, Wang Y, Wu D, Li T, Wang HD, Guo LJ, Guo QN, Xiao H, Lyu X, Yu ZH. Liu HY, et al. Among authors: li t. Chin Med J (Engl). 2017 Jan 5;130(1):104-107. doi: 10.4103/0366-6999.196568. Chin Med J (Engl). 2017. PMID: 28051032 Free PMC article. No abstract available.

9

[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.

10

[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.

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