Wang T - Search Results

1

[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: wang h, wang 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.

2

[The EXT2 gene mutation in a family with hereditary multiple exostoses].

Yao F, Wang Y, Liao S, Wang L, Wang T, Kang B. Yao F, et al. Among authors: wang l, wang y, wang t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Feb;27(1):92-5. doi: 10.3760/cma.j.issn.1003-9406.2010.01.020. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20140877 Chinese.

3

[Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome].

Wu D, Wang H, Zhang H, Hou Q, Qin L, Wang T, Xiao H, Liao S, Wang Y. Wu D, et al. Among authors: wang h, wang y, wang t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Dec;32(6):823-6. doi: 10.3760/cma.j.issn.1003-9406.2015.06.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26663057 Chinese.

4

Clinical and molecular cytogenetic analyses of four patients with imbalanced translocations.

Liu HY, Huang J, Li T, Wu D, Wang HD, Wang Y, Wang T, Guo LJ, Guo QN, Huang FF, Wang RL, Wang YT. Liu HY, et al. Among authors: wang hd, wang yt, wang y, wang t, wang rl. Mol Cytogenet. 2016 Apr 19;9:31. doi: 10.1186/s13039-016-0244-x. eCollection 2016. Mol Cytogenet. 2016. PMID: 27099631 Free PMC article.

5

[Phenotypic and genetic analysis of a child featuring multiple malformations due to chromosome 14q deletion].

Wang H, Wu D, Qin L, Wang T, Zhang H, Xing M, Liao S. Wang H, et al. Among authors: wang t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Jun;33(3):361-4. doi: 10.3760/cma.j.issn.1003-9406.2016.03.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27264822 Chinese.

6

[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: wang h, wang 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.

7

Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report.

Wu D, Zhang H, Hou Q, Wang H, Wang T, Liao S. Wu D, et al. Among authors: wang h, wang t. Mol Med Rep. 2017 Nov;16(5):6222-6227. doi: 10.3892/mmr.2017.7390. Epub 2017 Aug 29. Mol Med Rep. 2017. PMID: 28901405

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: wang h, wang 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

[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: wang x, wang 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.

10

[Prenatal diagnosis and genetic analysis of a fetus with endocardial cushion defects].

Wu D, Wang T, Hou Q, Li T, Wang X, Zhang C, Yang Y, Liu H, Liao S. Wu D, et al. Among authors: wang x, wang t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):418-421. doi: 10.3760/cma.j.issn.1003-9406.2018.03.025. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29896745 Chinese.

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