Kong XD - Search Results

1

A novel 3-base pair deletion of the CRYAA gene identified in a large Chinese pedigree featuring autosomal dominant congenital perinuclear cataract.

Kong XD, Liu N, Shi HR, Dong JM, Zhao ZH, Liu J, Li-Ling J, Yang YX. Kong XD, et al. Genet Mol Res. 2015 Jan 23;14(1):426-32. doi: 10.4238/2015.January.23.16. Genet Mol Res. 2015. PMID: 25729975 Free article.

2

[Haplotypes extending across AGT are associated essential hypertension].

Kong XD, Yang YX, Zhang SZ. Kong XD, et al. Yi Chuan. 2004 Nov;26(6):797-802. Yi Chuan. 2004. PMID: 15640105 Chinese.

3

[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: kong xd. 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.

4

[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: kong xd. 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.

5

[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: kong xd. 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.

6

[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: kong xd. Zhonghua Er Ke Za Zhi. 2012 Nov;50(11):851-4. Zhonghua Er Ke Za Zhi. 2012. PMID: 23302618 Chinese.

7

[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. 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.

8

[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: kong xd. 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.

9

[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. 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.

10

[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. Zhonghua Yi Xue Za Zhi. 2014 Apr 29;94(16):1227-31. Zhonghua Yi Xue Za Zhi. 2014. PMID: 24924886 Chinese.

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