Jiang M - Search Results

1

[Mutation analysis and first-trimester prenatal diagnosis for a Chinese family with hidrotic ectodermal dysplasia].

Liu N, Shi HR, Wu QH, Jiang M, Kong XD. Liu N, et al. Among authors: jiang m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):407-9. doi: 10.3760/cma.j.issn.1003-9406.2013.04.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23926005 Chinese.

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. Among authors: jiang m. 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. Among authors: jiang m. 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. Among authors: jiang m. 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. Among authors: jiang m. 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: jiang m. 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 analysis and prenatal diagnosis of keratin 9 gene in a large Chinese family with epidermolytic palmoplantar keratoderma].

Liu N, Shi H, Kong X, Wu Q, Jiang M. Liu N, et al. Among authors: jiang m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Feb;31(1):48-51. doi: 10.3760/cma.j.issn.1003-9406.2014.01.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24510562 Chinese.

8

[Mutation analysis of mucopolysaccharidosis type II and prenatal diagnosis].

Liu N, Shi H, Kong X, Wu Q, Jiang M. Liu N, et al. Among authors: jiang m. Zhonghua Fu Chan Ke Za Zhi. 2014 Jun;49(6):410-3. Zhonghua Fu Chan Ke Za Zhi. 2014. PMID: 25169630 Chinese.

9

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. Among authors: jiang m. 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

10

Mutation analysis and prenatal diagnosis in a Chinese family with succinic semialdehyde dehydrogenase and a systematic review of the literature of reported ALDH5A1 mutations.

Liu N, Kong XD, Kan QC, Shi HR, Wu QH, Zhuo ZH, Bai QL, Jiang M. Liu N, et al. Among authors: jiang m. J Perinat Med. 2016 May 1;44(4):441-51. doi: 10.1515/jpm-2014-0164. J Perinat Med. 2016. PMID: 25431891 Review.

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