Zhao Z - Search Results

1

Non-invasive prenatal testing of pregnancies at risk for phenylketonuria.

Duan H, Liu N, Zhao Z, Liu Y, Wang Y, Li Z, Xu M, Cram DS, Kong X. Duan H, et al. Among authors: zhao z. Arch Dis Child Fetal Neonatal Ed. 2019 Jan;104(1):F24-F29. doi: 10.1136/archdischild-2017-313929. Epub 2018 Jan 20. Arch Dis Child Fetal Neonatal Ed. 2019. PMID: 29353259

2

[Mutation analysis of phenylalanine hydroxylase gene in patients w ith phenylketonuria in Henan province].

GUO HJ, ZHAO ZH, JIANG M, SHI HR, KONG XD. GUO HJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Apr;28(2):142-6. doi: 10.3760/cma.j.issn.1003-9406.2011.02.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21462123 Chinese.

3

[Early prenatal genetic diagnosis of oculocutaneous albinism type I in seven families].

Wu Q, Shi HR, Liu N, Lu N, Jiang M, Zhao ZH, Kong XD. Wu Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):377-81. doi: 10.3760/cma.j.issn.1003-9406.2012.04.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875490 Chinese.

4

[Detection of ED1 gene mutations in six pedigrees with hypohidrotic ectodermal dysplasia].

Wu QH, Shi HR, Liu BC, Zhao ZH, Jiang M, Lu N, Kong XD. Wu QH, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):447-51. doi: 10.3760/cma.j.issn.1003-9406.2012.04.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875504 Chinese.

5

[Mutation analysis and prenatal diagnosis of a Chinese family with X-linked severe combined immunodeficiency].

Wu QH, Shi HR, Liu N, Jiang M, Lu N, Zhao ZH, Kong XD. Wu QH, et al. Zhonghua Er Ke Za Zhi. 2012 Nov;50(11):851-4. Zhonghua Er Ke Za Zhi. 2012. PMID: 23302618 Chinese.

6

[Mutation analysis of CRYBB1 gene and prenatal diagnosis for a Chinese kindred featuring autosomal dominant congenital nuclear cataract].

Wu Q, Shi H, Liu N, Lu N, Jiang M, Zhao Z, Kong X. Wu Q, et al. Among authors: zhao z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Jun;30(3):266-9. doi: 10.3760/cma.j.issn.1003-9406.2013.03.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23744311 Chinese.

7

[Mutation analyses and prenatal diagnosis in two families of X linked severe combined immunodeficiency caused by IL2RG gene novel mutation].

Kong X, Liu N, Xu X, Wu Q, Zhao Z, Bai Q, Meng J. Kong X, et al. Among authors: zhao z. Zhonghua Yi Xue Za Zhi. 2014 Apr 29;94(16):1227-31. Zhonghua Yi Xue Za Zhi. 2014. PMID: 24924886 Chinese.

8

Screening of human chromosome 21 genes in the dorsolateral prefrontal cortex of individuals with Down syndrome.

Kong XD, Liu N, Xu XJ, Zhao ZH, Jiang M. Kong XD, et al. Mol Med Rep. 2015 Feb;11(2):1235-9. doi: 10.3892/mmr.2014.2855. Epub 2014 Nov 4. Mol Med Rep. 2015. PMID: 25370074

9

[Mutation analysis of WASP gene and prenatal diagnosis of Wiskott-Aldrich syndrome].

Liu N, Shi H, Kong X, Wu Q, Xu X, Bai Q, Feng Y, Zhao Z. Liu N, et al. Among authors: zhao z. Zhonghua Er Ke Za Zhi. 2014 Sep;52(9):662-6. Zhonghua Er Ke Za Zhi. 2014. PMID: 25476427 Chinese.

10

[COL7A1 gene mutation analysis of dystrophic epidermolysis bullosa and prenatal diagnosis].

Liu N, Guo H, Kong X, Shi H, Yang Y, Wu Q, Zhao Z, Jiang M. Liu N, et al. Among authors: zhao z. Zhonghua Yi Xue Za Zhi. 2015 Jan 27;95(4):277-82. Zhonghua Yi Xue Za Zhi. 2015. PMID: 25877244 Chinese.

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