Zhao Y - Search Results

1

[Genetic diagnosis and noninvasive prenatal testing of a family with Williams-Beuren syndrome].

Zhao Y, Pang H, Feng X, Xiang Y, Gao M, Hua J, Tong D, Wu L, Sun H. Zhao Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):263-266. doi: 10.3760/cma.j.issn.1003-9406.2019.03.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30835361 Chinese.

2

[Analysis of genomic copy number variations in 36 fetuses with heart malformations using next-generation sequencing].

Gao M, Pang H, Zhao Y, Li-Ling J. Gao M, et al. Among authors: zhao y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):524-527. doi: 10.3760/cma.j.issn.1003-9406.2017.04.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777851 Chinese.

3

[Genetic diagnosis and follow up of a fetus with Emanuel syndrome].

Zhao Y, Pang H, Gao M, Feng X, Guan Y, Zhao H, Tong D, Hua J, Cao X, He S, Li-Ling J. Zhao Y, et al. Among authors: zhao h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Oct 10;34(5):709-713. doi: 10.3760/cma.j.issn.1003-9406.2017.05.020. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28981939 Chinese.

4

[Genetic diagnosis and non-invasive prenatal testing of a fetus with Prader-Willi/Angelman syndrome].

Gao M, Pang H, Shi Y, Feng X, Zhao Y, Hua J, Tong D, Liu J, Wen J, Fan T, Wu L. Gao M, et al. Among authors: zhao y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):543-546. doi: 10.3760/cma.j.issn.1003-9406.2019.06.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31055801 Chinese.

5

[Identification of cryptic structural chromosomal aberrations in parents through detection of copy number variations in miscarriage tissues].

Zhao Y, Pang H, Guo S, Cheng Z, Sun J, Lan C, Zhao Y, Sun R, Zhang M, Fan T, Yan X. Zhao Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1123-1126. doi: 10.3760/cma.j.issn.1003-9406.2019.11.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31703141 Chinese.

6

[Genetic analysis and prenatal diagnosis of a fetus with harlequin ichthyosis].

Yan X, Xiang Y, Huan D, Feng X, Zhao Y, Pang H. Yan X, et al. Among authors: zhao y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Dec 10;36(12):1195-1198. doi: 10.3760/cma.j.issn.1003-9406.2019.12.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31813146 Chinese.

7

[Prenatal diagnosis for two fetuses carrying partial deletion of Y chromosome].

Pang H, Gao M, Hua J, Tong D, Zhao Y, Feng X. Pang H, et al. Among authors: zhao y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Feb 10;37(2):182-185. doi: 10.3760/cma.j.issn.1003-9406.2020.02.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32034751 Chinese.

8

[Phenotypic analysis and variant identification of a fetus with Joubert syndrome 17].

Zhao Y, Zhao Y, Lyu Y, Pang H. Zhao Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Sep 10;38(9):841-844. doi: 10.3760/cma.j.cn511374-20200716-00520. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34487526 Chinese.

9

[Another grey zone for clinical genetics: chromosomal microduplication 22q11.2].

Zhao YH, Li Ling J. Zhao YH, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Oct;24(5):551-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17922425 Review. Chinese.

10

[Genetic analysis of genitourinary malformations].

Zhang JS, Fu Y, Zhao YH, Li F, Qian AL, Wu B, Li-Ling J. Zhang JS, et al. Among authors: zhao yh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Apr;26(2):134-8. doi: 10.3760/cma.j.issn.1003-9406.2009.02.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19350501 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

80,805 results

Search Page