Kong X - Search Results

1

[Application of Karyomapping for the prenatal diagnosis of five families affected with facioscapulohumerial muscular dystrophy type 1].

Zheng Y, Kong L, Xu H, Bai Z, Lu Y, Kong X. Zheng Y, et al. Among authors: kong x, kong l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):203-206. doi: 10.3760/cma.j.issn.1003-9406.2019.03.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30835346 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. 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

[A study on paternity testing with 96 autosomal SNPs].

Lee L, Wang L, Feng QC, Zhu YL, Cheng XL, Kong XD, Huang YM, Wang WF, Zeng ZS. Lee L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Feb;29(1):28-33. doi: 10.3760/cma.j.issn.1003-9406.2012.01.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22311487 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. 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. 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. 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. Among authors: kong x. 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. 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. Among authors: kong x. 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

Rapid diagnosis of aneuploidy using segmental duplication quantitative fluorescent PCR.

Kong X, Li L, Sun L, Fu K, Long J, Weng X, Ye X, Liu X, Wang B, Yan S, Ye H, Fan Z. Kong X, et al. PLoS One. 2014 Mar 13;9(3):e88932. doi: 10.1371/journal.pone.0088932. eCollection 2014. PLoS One. 2014. PMID: 24625828 Free PMC article.

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