Zhao G - Search Results

1

[Genetic testing and prenatal diagnosis for a Chinese pedigree affected with mitochondrial DNA depletion syndrome due to variant of MPV17 gene].

Zhao G, Zhao X, Zhao X, Liu L, Wang C, Kong X. Zhao G, et al. Among authors: zhao x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Oct 10;39(10):1085-1088. doi: 10.3760/cma.j.cn511374-20210718-00604. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36184088 Chinese.

2

Novel mutations of COL4A3, COL4A4, and COL4A5 genes in Chinese patients with Alport Syndrome using next generation sequence technique.

Zhao X, Chen C, Wei Y, Zhao G, Liu L, Wang C, Zhang J, Kong X. Zhao X, et al. Among authors: zhao g. Mol Genet Genomic Med. 2019 Jun;7(6):e653. doi: 10.1002/mgg3.653. Epub 2019 Apr 9. Mol Genet Genomic Med. 2019. PMID: 30968591 Free PMC article.

3

A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing.

Zhao G, Dai P, Gao S, Zhao X, Wang C, Liu L, Kong X. Zhao G, et al. Among authors: zhao x. Mol Cytogenet. 2019 Dec 21;12:53. doi: 10.1186/s13039-019-0464-y. eCollection 2019. Mol Cytogenet. 2019. PMID: 31890033 Free PMC article.

4

Identification of four novel mutations in the COL4A5 gene identified in Chinese patients with X-linked Alport syndrome.

Zhao X, Shang X, Chen C, Liu L, Wang C, Zhao G, Zhang J, Kong X. Zhao X, et al. Among authors: zhao g. Biomed Rep. 2020 Aug;13(2):4. doi: 10.3892/br.2020.1311. Epub 2020 Jun 9. Biomed Rep. 2020. PMID: 32607233 Free PMC article.

5

[Spectrum of pathological genetic variants among 405 Chinese pedigrees affected with oculocutaneous albinism].

Wang C, Chen C, Zhao X, Zhao G, Liu L, Kong X. Wang C, et al. Among authors: zhao x, zhao g. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jul 10;37(7):725-730. doi: 10.3760/cma.j.issn.1003-9406.2020.07.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32619251 Chinese.

6

Identification of two novel SMN1 point mutations associated with a very severe SMA-I phenotype.

Zhao X, Wang Y, Mei S, Chen C, Liu L, Wang C, Zhao G, Kong X. Zhao X, et al. Among authors: zhao g. Eur J Med Genet. 2020 Sep;63(9):104006. doi: 10.1016/j.ejmg.2020.104006. Epub 2020 Jul 10. Eur J Med Genet. 2020. PMID: 32659294

7

[Application of bionano optical mapping for the diagnosis of a 16p11.2-p12.2 microdeletion].

Dai P, Zhu C, Zhao G, Dong X. Dai P, et al. Among authors: zhao g. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Oct 10;37(10):1167-1171. doi: 10.3760/cma.j.cn511374-20190906-00458. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32924127 Chinese.

8

Clinical Significance of Non-Invasive Prenatal Screening for Trisomy 7: Cohort Study and Literature Review.

Zhu X, Lam DYM, Chau MHK, Xue S, Dai P, Zhao G, Cao Y, Cheung SWH, Kwok YKY, Choy KW, Kong X, Leung TY. Zhu X, et al. Among authors: zhao g. Genes (Basel). 2020 Dec 24;12(1):11. doi: 10.3390/genes12010011. Genes (Basel). 2020. PMID: 33374124 Free PMC article. Review.

9

[Results of non-invasive prenatal testing for 2473 women with twin pregnancy].

Chen S, Dai P, Zhao G, Zhang F, Guo W, Gao S, Kong X. Chen S, et al. Among authors: zhao g. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Apr 10;38(4):313-316. doi: 10.3760/cma.j.cn511374-20200521-00368. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33834454 Chinese.

10

[Non-invasive prenatal detection of ocutaneous albinism type I based on cfDNA barcode-enabled single-molecule test].

Wang C, Chen C, Wang X, Zhao X, Zhao G, Liu L, Kong X. Wang C, et al. Among authors: zhao x, zhao g. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Apr 10;38(4):317-320. doi: 10.3760/cma.j.cn511374-20200214-00077. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33834455 Chinese.

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