Gao M - Search Results

1

Applications of noninvasive prenatal testing in vanishing twin syndrome pregnancies after treatment of assisted reproductive technology in a single center.

Zou Y, Cui L, Xue M, Yan J, Huang M, Gao M, Gao X, Gao Y, Chen ZJ. Zou Y, et al. Among authors: gao x, gao y, gao m. Prenat Diagn. 2021 Jan;41(2):226-233. doi: 10.1002/pd.5836. Epub 2020 Nov 30. Prenat Diagn. 2021. PMID: 33009680

2

[A novel pathogenic mutation of CRYGD gene in a congenital cataract family].

Gao M, Huang S, Li J, Zou Y, Xu P, Kang R, Gao Y. Gao M, et al. Among authors: gao y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Aug;33(4):515-8. doi: 10.3760/cma.j.issn.1003-9406.2016.04.020. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27455011 Chinese.

3

[Application of droplet digital PCR technology for genetic testing and prenatal diagnosis of spinal muscular atrophy].

Zou Y, Xu P, Li J, Huang S, Gao M, Kang R, Gao X, Gao Y. Zou Y, et al. Among authors: gao x, gao y, gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Oct;33(5):594-7. doi: 10.3760/cma.j.issn.1003-9406.2016.05.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27577201 Chinese.

4

[Identification of a novel splicing mutation of PKD1 gene in a pedigree affected with autosomal dominant polycystic kidney disease].

Xu P, Zou Y, Li J, Huang S, Gao M, Kang R, Gao Y. Xu P, et al. Among authors: gao y, gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Dec 10;33(6):778-781. doi: 10.3760/cma.j.issn.1003-9406.2016.06.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27984604 Chinese.

5

[Identification of a novel splicing mutation of PHEX gene in a pedigree affected with X-linked hypophosphatemia].

Li J, Xu P, Huang S, Gao M, Zou Y, Kang R, Gao Y. Li J, et al. Among authors: gao y, gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):216-219. doi: 10.3760/cma.j.issn.1003-9406.2017.02.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397222 Chinese.

6

[A novel mutation of GLI3 gene underlying synpolydactyly in a family].

Kang R, Huang S, Li J, Zou Y, Xu P, Gao M, Wang L, Xie H, Yan J, Gao Y. Kang R, et al. Among authors: gao y, gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):490-493. doi: 10.3760/cma.j.issn.1003-9406.2017.04.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777844 Chinese.

7

[Application of droplet digital PCR for non-invasive prenatal diagnosis of single gene disease in two families].

Xu P, Zou Y, Li J, Huang S, Gao M, Kang R, Xie H, Wang L, Yan J, Gao Y. Xu P, et al. Among authors: gao y, gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):224-227. doi: 10.3760/cma.j.issn.1003-9406.2018.02.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29652997 Chinese.

8

[Novel mutations of XPC gene detected in a family affected with xeroderma pigmentosum group C].

Wang L, Huang S, Li J, Zou Y, Xu P, Gao M, Kang R, Xie H, Wei X, Niu Y, Liu X, Gao Y. Wang L, et al. Among authors: gao y, gao m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):540-543. doi: 10.3760/cma.j.issn.1003-9406.2018.04.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098252 Chinese.

9

A novel splicing mutation in the PKD1 gene causes autosomal dominant polycystic kidney disease in a Chinese family: a case report.

Xu P, Huang S, Li J, Zou Y, Gao M, Kang R, Yan J, Gao X, Gao Y. Xu P, et al. Among authors: gao x, gao y, gao m. BMC Med Genet. 2018 Nov 13;19(1):198. doi: 10.1186/s12881-018-0706-6. BMC Med Genet. 2018. PMID: 30424739 Free PMC article.

10

Novel mutation of EDA causes new asymmetrical X-linked hypohidrotic ectodermal dysplasia phenotypes in a female.

Shen L, Liu C, Gao M, Li H, Zhang Y, Tian Q, Ni H, Peng P, Zhao R, Hu Z, Gao Y, Xia K, Bo Q, Guo H. Shen L, et al. Among authors: gao y, gao m. J Dermatol. 2019 Aug;46(8):731-733. doi: 10.1111/1346-8138.14978. Epub 2019 Jun 26. J Dermatol. 2019. PMID: 31241787

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