Chen Y - Search Results

1

A novel mutation (C1425Y) in the FBN2 gene in a father and son with congenital contractural arachnodactyly.

Chen Y, Lei YP, Zheng HX, Wang W, Cheng HB, Zhang J, Wang HY, Jin L, Li H. Chen Y, et al. Genet Test Mol Biomarkers. 2009 Jun;13(3):295-300. doi: 10.1089/gtmb.2008.0132. Genet Test Mol Biomarkers. 2009. PMID: 19473076

2

[Analysis of GJB2 gene and mitochondrial DNA A1555G mutations in 16 families with non-syndromic hearing loss].

Wang W, Cheng HB, Yang N, Shi YC, Liu JZ, Li Q, Yang SM, Shen LY, Liu MJ, Chen Y, Li H. Wang W, et al. Among authors: chen y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):388-92. doi: 10.3760/cma.j.issn.1003-9406.2012.04.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875492 Chinese.

3

[SLC26A4 mutations in a Chinese deafness family discovered by next-generation sequencing technology].

Mao J, Wei XM, Li H, Wang SN, Chen Y. Mao J, et al. Among authors: chen y. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Nov;47(11):942-5. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23302201 Chinese.

4

Quantitative trait analysis of polymorphisms in two bilirubin metabolism enzymes to physiologic bilirubin levels in Chinese newborns.

Zhou Y, Wang SN, Li H, Zha W, Peng Q, Li S, Chen Y, Jin L. Zhou Y, et al. Among authors: chen y. J Pediatr. 2014 Dec;165(6):1154-1160.e1. doi: 10.1016/j.jpeds.2014.08.041. Epub 2014 Sep 26. J Pediatr. 2014. PMID: 25262300

5

Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants.

Zhou Y, Wang SN, Li H, Zha W, Wang X, Liu Y, Sun J, Peng Q, Li S, Chen Y, Jin L. Zhou Y, et al. Among authors: chen y. PLoS One. 2014 Aug 7;9(8):e104251. doi: 10.1371/journal.pone.0104251. eCollection 2014. PLoS One. 2014. PMID: 25102181 Free PMC article.

6

[A literature review of epidemiological studies on mutation hot spots of Chinese population with non-syndromic hearing loss].

Li H, Li Q, Li H, Chen Y. Li H, et al. Among authors: chen y. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Jul;26(13):589-94. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23002642 Review. Chinese.

7

Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.

Wang B, Liu M, Yan W, Mao J, Jiang D, Li H, Chen Y. Wang B, et al. Among authors: chen y. J Matern Fetal Neonatal Med. 2013 Dec;26(18):1768-77. doi: 10.3109/14767058.2013.799648. Epub 2013 Jun 10. J Matern Fetal Neonatal Med. 2013. PMID: 23701284

8

[A microdeletion of chromosome 9q34.11 may cause suspected cerebral palsy].

Li H, Chen Y, Li Q, Liu M, Mao J, Song D, Li H. Li H, et al. Among authors: chen y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):725-9. doi: 10.3760/cma.j.issn.1003-9406.2014.06.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449075 Chinese.

9

A patient with five chromosomal rearrangements and a 2q31.1 microdeletion.

Wang T, Mao J, Liu MJ, Choy KW, Li HB, Cram DS, Li H, Chen Y. Wang T, et al. Among authors: chen y. Clin Chim Acta. 2014 Mar 20;430:129-33. doi: 10.1016/j.cca.2014.01.002. Epub 2014 Jan 9. Clin Chim Acta. 2014. PMID: 24412318

10

Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.

Mao J, Wang T, Wang BJ, Liu YH, Li H, Zhang J, Cram D, Chen Y. Mao J, et al. Among authors: chen y. Clin Chim Acta. 2014 Jun 10;433:190-3. doi: 10.1016/j.cca.2014.03.011. Epub 2014 Mar 22. Clin Chim Acta. 2014. PMID: 24667696

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