Chen Y - Search Results

1

[Genetic analysis of a family with super-male syndrome].

Zhang J, Li H, Jiang S, Chen Y, Zhang Y. Zhang J, et al. Among authors: chen y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Apr;31(2):210-3. doi: 10.3760/cma.j.issn.1003-9406.2014.02.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24711034 Chinese.

2

[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.

3

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

4

[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.

5

[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.

6

[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.

7

[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.

8

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

9

MicroRNA-200b is overexpressed in endometrial adenocarcinomas and enhances MMP2 activity by downregulating TIMP2 in human endometrial cancer cell line HEC-1A cells.

Dai Y, Xia W, Song T, Su X, Li J, Li S, Chen Y, Wang W, Ding H, Liu X, Li H, Zhao Q, Shao N. Dai Y, et al. Among authors: chen y. Nucleic Acid Ther. 2013 Feb;23(1):29-34. doi: 10.1089/nat.2012.0385. Epub 2012 Dec 3. Nucleic Acid Ther. 2013. PMID: 23205572 Free PMC article.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

179,973 results

Search Page

Filters