Zhao X - Search Results

1

[Analysis of NF1 gene mutations in two sporadic patients with neurofibromatosis type 1].

Zhao X, Zhou Q, Cai L, Zhao Z, Zhang L, Wang P, Zhang G. Zhao X, et al. Among authors: zhao z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):489-492. doi: 10.3760/cma.j.issn.1003-9406.2018.04.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098240 Chinese.

2

[Mutation analysis of STK11 gene in a Chinese family with Peutz-Jeghers syndrome].

Zhao X, Huang Y, Yang B, Zhao Y. Zhao X, et al. Among authors: zhao y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):294-7. doi: 10.3760/cma.j.issn.1003-9406.2014.03.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24928005 Chinese.

3

[Analysis of ATP2A2 gene mutations in a pedigree and a sporadic case with Darier disease].

Zhao X, Gu Y, Du X, Shao M, Luo H, Zhu L, Zhou Q, Zhang G. Zhao X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Oct;33(5):641-4. doi: 10.3760/cma.j.issn.1003-9406.2016.05.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27577212 Chinese.

4

Identification of a novel mutation in the mechanoreceptor-encoding gene CXCR1 in patients with keloid.

Zhang Q, Cai L, Wang M, Ke X, Zhao X, Huang Y. Zhang Q, et al. Among authors: zhao x. Arch Dermatol Res. 2018 Sep;310(7):561-566. doi: 10.1007/s00403-018-1847-3. Epub 2018 Jun 21. Arch Dermatol Res. 2018. PMID: 29931443 Free PMC article.

5

[Analysis of NF1 gene variant in a sporadic case with neurofibromatosis type 1].

Zhao X, Cai L, Zhang L, Wang P, Zhang G. Zhao X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Aug 10;37(8):871-874. doi: 10.3760/cma.j.issn.1003-9406.2020.08.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32761598 Chinese.

6

[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.

7

[Analysis of NF1 gene variants in a Chinese pedigree and a sporadic patient with Neurofibromatosis type 1].

Zhao X, Zhou K, Zhang Q, Cai L. Zhao X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Mar 10;41(3):317-321. doi: 10.3760/cma.j.cn511374-20221123-00811. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 38448021 Chinese.

8

[Analysis of a Chinese pedigree affected with Meckel syndrome due to variants of TMEM67 gene].

Zhao G, Zhao X, Zhao X, Wang C, Jiao Z, Li Q, Kong X. Zhao G, et al. Among authors: zhao x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Oct 10;40(10):1236-1240. doi: 10.3760/cma.j.cn511374-20210626-00544. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37730223 Chinese.

9

[Analysis of a twin pregnancy with false negative result for 22q11.2 deletion syndrome by expanded non-invasive prenatal testing].

Zhao G, Jiao Z, Dai P, Zhao X, Kong X. Zhao G, et al. Among authors: zhao x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Dec 10;40(12):1451-1454. doi: 10.3760/cma.j.cn511374-20210628-00551. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37994122 Chinese.

10

Two novel TSC2 mutations in Chinese patients with tuberous sclerosis complex and a literature review of 20 patients reported in China.

Zhao XY, Yang S, Zhou HL, Zhu YG, Wei L, Du WH, Ren YQ, Liang YH, Hou YX, Chen JJ, Zhang XJ. Zhao XY, et al. Br J Dermatol. 2006 Nov;155(5):1070-3. doi: 10.1111/j.1365-2133.2006.07469.x. Br J Dermatol. 2006. PMID: 17034546 Review. No abstract available.

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