Liu Y - Search Results

1

[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. Among authors: liu y. 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.

2

[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. Among authors: liu y. 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.

3

[Establishment of medians for maternal serum markers in Down's syndrome screening during the second trimester of pregnancy in north-central region of Jiangxi Province].

Long Y, Liu Y, Ma P, You X, Yuan H. Long Y, et al. Among authors: liu y. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2017 Jul 28;42(7):831-835. doi: 10.11817/j.issn.1672-7347.2017.07.015. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2017. PMID: 28845009 Free article. Chinese.

4

[Study of the phenylalanine hydroxylase gene variants in patients with phenylketonuria from Jiangxi province].

Lu Q, Liu Y, Yang B, Xie K, Zou Y, Lu W, Wang F. Lu Q, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1057-1061. doi: 10.3760/cma.j.issn.1003-9406.2019.11.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31703125 Chinese.

5

[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. Among authors: liu y. 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.

6

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: liu 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.

7

[The value of combined use of chromosomal karyotyping and chromosome microarray analysis for prenatal diagnosis].

Rao H, Liu Y, Lu Q, Huang N, Zhou J. Rao H, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Apr 10;37(4):392-396. doi: 10.3760/cma.j.issn.1003-9406.2020.04.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32219820 Chinese.

8

[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. Among authors: liu y. 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.

9

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: liu yq, liu dp. 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.

10

[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: liu 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.

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