Yang Y - Search Results

1

[Comparison of results of improved FISH and conventional karyotyping analysis of 2607 amniotic fluid samples].

Yang Y, Liu Y, Huang N, Xie K. Yang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Dec;32(6):785-8. doi: 10.3760/cma.j.issn.1003-9406.2015.06.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26663048 Chinese.

2

[Application of NGS-based SNP haplotyping for preimplantation genetic diagnosis for beta-thalassemia and HLA matching].

Yang Y, Liu Y, Lu Q, Chen J, Luo H, Ma P. Yang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1090-1093. doi: 10.3760/cma.j.issn.1003-9406.2019.11.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31703132 Chinese.

3

A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family.

Chen J, Yuan H, Xie K, Wang X, Tan L, Zou Y, Yang Y, Pan L, Xiao J, Chen G, Liu Y. Chen J, et al. Among authors: yang y. BMC Cardiovasc Disord. 2020 Jan 20;20(1):27. doi: 10.1186/s12872-019-01322-1. BMC Cardiovasc Disord. 2020. PMID: 31959127 Free PMC article.

4

[Application of next generation sequencing for preimplantation genetic test of 71 couples with one partner carrying a reciprocal or Robertsonian translocation].

Yang Y, Liu Y, Ma P, Chen J, Ding T. Yang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 May 10;37(5):563-566. doi: 10.3760/cma.j.issn.1003-9406.2020.05.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32335887 Chinese.

5

[Analysis of a pedigree affected with propionic acidemia by trio whole exome sequencing].

Yang Y, Liu Y, Chen J, Luo H. Yang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jul 10;37(7):751-754. doi: 10.3760/cma.j.issn.1003-9406.2020.07.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32619257 Chinese.

6

Next-generation sequencing: a follow-up of 36,913 singleton pregnancies with noninvasive prenatal testing in central China.

Lu W, Huang T, Wang XR, Zhou JH, Yuan HZ, Yang Y, Huang TT, Liu DP, Liu YQ. Lu W, et al. Among authors: yang y. J Assist Reprod Genet. 2020 Dec;37(12):3143-3150. doi: 10.1007/s10815-020-01977-2. Epub 2020 Oct 23. J Assist Reprod Genet. 2020. PMID: 33094428 Free PMC article.

7

[Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with N-acetylglutamate synthase deficiency].

Chen J, Yuan H, Xie K, Guo Z, Yang Y, Zou Y, Chen G, Liu Y. Chen J, et al. Among authors: yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Dec 10;37(12):1360-1363. doi: 10.3760/cma.j.cn511374-20200203-00055. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 33306822 Chinese.

8

Identification of a Novel Nonsense Mutation in PLA2G6 and Prenatal Diagnosis in a Chinese Family With Infantile Neuroaxonal Dystrophy.

Zou Y, Luo H, Yuan H, Xie K, Yang Y, Huang S, Yang B, Liu Y. Zou Y, et al. Among authors: yang b, yang y. Front Neurol. 2022 Jul 6;13:904027. doi: 10.3389/fneur.2022.904027. eCollection 2022. Front Neurol. 2022. PMID: 35873758 Free PMC article.

9

Molecular prevalence of HBB-associated hemoglobinopathy among reproductive-age adults and the prenatal diagnosis in Jiangxi Province, southern central China.

Luo H, Huang T, Lu Q, Zhang L, Xu Y, Yang Y, Guo Z, Yuan H, Shen Y, Huang S, Yang B, Zou Y, Liu Y. Luo H, et al. Among authors: yang b, yang y. Front Genet. 2022 Sep 28;13:992073. doi: 10.3389/fgene.2022.992073. eCollection 2022. Front Genet. 2022. PMID: 36246595 Free PMC article.

10

Performance of expanded non-invasive prenatal testing for fetal aneuploidies and copy number variations: A prospective study from a single center in Jiangxi province, China.

Zou Y, Feng C, Qin J, Wang X, Huang T, Yang Y, Xie K, Yuan H, Huang S, Yang B, Lu W, Liu Y. Zou Y, et al. Among authors: yang b, yang y. Front Genet. 2023 Jan 13;13:1073851. doi: 10.3389/fgene.2022.1073851. eCollection 2022. Front Genet. 2023. PMID: 36712884 Free PMC article.

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