Wang T - Search Results

1

Prenatal Diagnosis and Genetic Analysis of a Fetus with Joubert Syndrome.

Xiang J, Zhang L, Jiang W, Zhang Q, Wang T, Li H, Li H. Xiang J, et al. Among authors: wang t. Biomed Res Int. 2018 May 31;2018:7202168. doi: 10.1155/2018/7202168. eCollection 2018. Biomed Res Int. 2018. PMID: 29955609 Free PMC article.

2

[Prenatal diagnosis of a fetus with cleft lip and palate by using chromosomal microarray analysis].

Huang C, Song X, Zhang Q, Liu M, Mao J, Xiang J, Liu Y, Li H, Wang T. Huang C, et al. Among authors: wang t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Apr 10;37(4):471-474. doi: 10.3760/cma.j.issn.1003-9406.2020.04.027. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32219840 Chinese.

3

An Optimized Method for Accurate Fetal Sex Prediction and Sex Chromosome Aneuploidy Detection in Non-Invasive Prenatal Testing.

Wang T, He Q, Li H, Ding J, Wen P, Zhang Q, Xiang J, Li Q, Xuan L, Kong L, Mao Y, Zhu Y, Shen J, Liang B, Li H. Wang T, et al. PLoS One. 2016 Jul 21;11(7):e0159648. doi: 10.1371/journal.pone.0159648. eCollection 2016. PLoS One. 2016. PMID: 27441628 Free PMC article.

4

Identification of a novel nonsense mutation of the neurotrophic tyrosine kinase receptor type 1 gene in two siblings with congenital insensitivity to pain with anhidrosis.

Wang T, Li H, Xiang J, Wei B, Zhang Q, Zhu Q, Liu M, Sun M, Li H. Wang T, et al. J Int Med Res. 2017 Apr;45(2):549-555. doi: 10.1177/0300060517691699. Epub 2017 Mar 27. J Int Med Res. 2017. PMID: 28345382 Free PMC article.

5

[Two false negative cases in noninvasive prenatal testing for fetal chromosomal aneuploidies].

Wen P, Xue Y, Zhang Q, Liang Q, Li Q, Li H, Ding J, Li H, Wang T. Wen P, et al. Among authors: wang t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):884-887. doi: 10.3760/cma.j.issn.1003-9406.2017.06.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188622 Chinese.

6

Human oocyte maturation arrest caused by a novel missense mutation in TUBB8.

Xiang J, Wang W, Qian C, Xue J, Wang T, Li H, Li H. Xiang J, et al. Among authors: wang w, wang t. J Int Med Res. 2018 Sep;46(9):3759-3764. doi: 10.1177/0300060518778638. Epub 2018 Jun 7. J Int Med Res. 2018. PMID: 29877102 Free PMC article.

7

Noninvasive Prenatal Screening for Fetal Sex Chromosome Aneuploidies at Two Next-Generation Sequencing Platforms.

Xue Y, Li H, Zhang Q, Zhao G, Ding J, Shen C, Qiao L, Wang T. Xue Y, et al. Among authors: wang t. Ann Clin Lab Sci. 2018 Jul;48(4):501-505. Ann Clin Lab Sci. 2018. PMID: 30143493

8

Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 Pregnancies.

Xiang J, Ding Y, Song X, Mao J, Liu M, Liu Y, Huang C, Zhang Q, Wang T. Xiang J, et al. Among authors: wang t. Front Genet. 2020 Nov 6;11:571219. doi: 10.3389/fgene.2020.571219. eCollection 2020. Front Genet. 2020. PMID: 33240322 Free PMC article.

9

[Genetic testing and prenatal diagnosis for a pedigree affected with tuberous sclerosis complex].

Huang C, Zhang Q, Xue Y, Li H, Wang T. Huang C, et al. Among authors: wang t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Feb 10;38(2):154-157. doi: 10.3760/cma.j.cn511374-20200331-00227. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33565070 Chinese.

10

Whole Exome Sequencing Aids the Diagnosis of Fetal Skeletal Dysplasia.

Tang H, Zhang Q, Xiang J, Yin L, Wang J, Wang T. Tang H, et al. Among authors: wang j, wang t. Front Genet. 2021 Mar 10;12:599863. doi: 10.3389/fgene.2021.599863. eCollection 2021. Front Genet. 2021. PMID: 33777089 Free PMC article.

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