Lu Y - Search Results

1

[Genetic and audiological characters of a Chinese family with non-syndromic hereditary hearing loss].

Jin Z, Cheng J, Lu Y, Li J, Sun Y, Yuan H, Han D. Jin Z, et al. Among authors: lu y. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011 Feb;25(4):158-61. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011. PMID: 21563462 Chinese.

2

Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China.

Sun Y, Chen J, Sun H, Cheng J, Li J, Lu Y, Lu Y, Jin Z, Zhu Y, Ouyang X, Yan D, Dai P, Han D, Yang W, Wang R, Liu X, Yuan H. Sun Y, et al. Among authors: lu y. J Hum Genet. 2011 Jan;56(1):64-70. doi: 10.1038/jhg.2010.147. Epub 2010 Dec 9. J Hum Genet. 2011. PMID: 21150918

3

Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss.

Li J, Cheng J, Lu Y, Lu Y, Chen A, Sun Y, Kang D, Zhang X, Dai P, Han D, Yuan H. Li J, et al. Among authors: lu y. J Genet Genomics. 2010 Dec;37(12):787-93. doi: 10.1016/S1673-8527(09)60096-5. J Genet Genomics. 2010. PMID: 21193157

4

Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss.

Sun Y, Cheng J, Lu Y, Li J, Lu Y, Jin Z, Dai P, Wang R, Yuan H. Sun Y, et al. Among authors: lu y. J Genet Genomics. 2011 Feb;38(2):71-6. doi: 10.1016/j.jcg.2011.01.001. Epub 2011 Feb 23. J Genet Genomics. 2011. PMID: 21356526

5

[Characteristics of audiology and clinical genetics of a Chinese family with the DFNA5 genetic hearing loss].

Jin Z, Cheng J, Han B, Li H, Lu Y, Li Z, Han D. Jin Z, et al. Among authors: lu y. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011 May;25(9):395-8. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011. PMID: 21805831 Chinese.

6

[Clinical and genetic features of a large Chinese family with nonsyndromic autosomal dominant hearing loss].

Li H, Cheng J, Lu Y, Li Z, Jia J, Yuan H, Han D. Li H, et al. Among authors: lu y. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 May;26(9):414-7, 421. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 22803410 Chinese.

7

[Clinical and genetic analysis of a patient with Treacher Collins syndrome in TCOF1 gene].

Li H, Zhang X, Li Z, Chen J, Lu Y, Jia J, Yuan H, Han D. Li H, et al. Among authors: lu y. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 May;26(10):459-62. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 22870720 Chinese.

8

Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family.

Gao X, Su Y, Guan LP, Yuan YY, Huang SS, Lu Y, Wang GJ, Han MY, Yu F, Song YS, Zhu QY, Wu J, Dai P. Gao X, et al. Among authors: lu y. PLoS One. 2013 May 14;8(5):e63026. doi: 10.1371/journal.pone.0063026. Print 2013. PLoS One. 2013. PMID: 23690975 Free PMC article.

9

Identification of a Novel TECTA mutation in a Chinese DFNA8/12 family with prelingual progressive sensorineural hearing impairment.

Li Z, Guo Y, Lu Y, Li J, Jin Z, Li H, Lu Y, Dai P, Han D, Cheng J, Yuan H. Li Z, et al. Among authors: lu y. PLoS One. 2013 Jul 31;8(7):e70134. doi: 10.1371/journal.pone.0070134. Print 2013. PLoS One. 2013. PMID: 23936151 Free PMC article.

10

Preimplantation genetic diagnosis for a Chinese family with autosomal recessive Meckel-Gruber syndrome type 3 (MKS3).

Lu Y, Peng H, Jin Z, Cheng J, Wang S, Ma M, Lu Y, Han D, Yao Y, Li Y, Yuan H. Lu Y, et al. PLoS One. 2013 Sep 5;8(9):e73245. doi: 10.1371/journal.pone.0073245. eCollection 2013. PLoS One. 2013. PMID: 24039893 Free PMC article.

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