Chen Y - Search Results

1

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

2

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

3

[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.

4

Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss.

Chen Y, Liu Y, Wang B, Mao J, Wang T, Ye K, Ye Y, Cram DS, Li H. Chen Y, et al. Prenat Diagn. 2016 Dec;36(13):1233-1241. doi: 10.1002/pd.4962. Epub 2016 Dec 9. Prenat Diagn. 2016. PMID: 27862068

5

[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.

6

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 Free article.

7

[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.

8

Methylenetetrahydrofolate reductase polymorphisms at 3'-untranslated region are associated with susceptibility to preterm birth.

Zhu Q, Chen Y, Dai J, Wang B, Liu M, Wang Y, Tao J, Li H. Zhu Q, et al. Among authors: chen y. Transl Pediatr. 2015 Jan;4(1):57-62. doi: 10.3978/j.issn.2224-4336.2015.01.02. Transl Pediatr. 2015. PMID: 26835361 Free PMC article.

9

[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.

10

[Multicenter investigation on the impact of newborn infants' gestational age and birth weight on the level of 17α-hydroxyprogesterone].

Zhang Q, Wang B, Chen Y, Jiang D, Chen Y. Zhang Q, et al. Among authors: chen y. Zhonghua Er Ke Za Zhi. 2014 Sep;52(9):706-9. Zhonghua Er Ke Za Zhi. 2014. PMID: 25476436 Chinese.

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