Wu BL - Search Results

1

Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.

Dai P, Stewart AK, Chebib F, Hsu A, Rozenfeld J, Huang D, Kang D, Lip V, Fang H, Shao H, Liu X, Yu F, Yuan H, Kenna M, Miller DT, Shen Y, Yang W, Zelikovic I, Platt OS, Han D, Alper SL, Wu BL. Dai P, et al. Among authors: wu bl. Physiol Genomics. 2009 Aug 7;38(3):281-90. doi: 10.1152/physiolgenomics.00047.2009. Epub 2009 Jun 9. Physiol Genomics. 2009. PMID: 19509082

2

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss.

Dai P, Li Q, Huang D, Yuan Y, Kang D, Miller DT, Shao H, Zhu Q, He J, Yu F, Liu X, Han B, Yuan H, Platt OS, Han D, Wu BL. Dai P, et al. Among authors: wu bl. Genet Med. 2008 Aug;10(8):586-92. doi: 10.1097/gim.0b013e31817d2ef1. Genet Med. 2008. PMID: 18641518

3

GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment.

Dai P, Yu F, Han B, Liu X, Wang G, Li Q, Yuan Y, Liu X, Huang D, Kang D, Zhang X, Yuan H, Yao K, Hao J, He J, He Y, Wang Y, Ye Q, Yu Y, Lin H, Liu L, Deng W, Zhu X, You Y, Cui J, Hou N, Xu X, Zhang J, Tang L, Song R, Lin Y, Sun S, Zhang R, Wu H, Ma Y, Zhu S, Wu BL, Han D, Wong LJ. Dai P, et al. Among authors: wu h, wu bl. J Transl Med. 2009 Apr 14;7:26. doi: 10.1186/1479-5876-7-26. J Transl Med. 2009. PMID: 19366456 Free PMC article.

4

[Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients].

Dai P, Yu F, Kang DY, Zhang X, Liu X, Mi WZ, Cao JY, Yuan HJ, Yang WY, Wu BL, Han DY. Dai P, et al. Among authors: wu bl. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005 Oct;40(10):769-73. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005. PMID: 16408730 Chinese.

5

Designing a simple multiplex ligation-dependent probe amplification (MLPA) assay for rapid detection of copy number variants in the genome.

Shen Y, Wu BL. Shen Y, et al. Among authors: wu bl. J Genet Genomics. 2009 Apr;36(4):257-65. doi: 10.1016/S1673-8527(08)60113-7. J Genet Genomics. 2009. PMID: 19376486

6

Detection of copy number variants reveals association of cilia genes with neural tube defects.

Chen X, Shen Y, Gao Y, Zhao H, Sheng X, Zou J, Lip V, Xie H, Guo J, Shao H, Bao Y, Shen J, Niu B, Gusella JF, Wu BL, Zhang T. Chen X, et al. Among authors: wu bl. PLoS One. 2013;8(1):e54492. doi: 10.1371/journal.pone.0054492. Epub 2013 Jan 17. PLoS One. 2013. PMID: 23349908 Free PMC article.

7

Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafness.

Wu BL, Kenna M, Lip V, Irons M, Platt O. Wu BL, et al. Am J Med Genet A. 2003 Aug 30;121A(2):102-8. doi: 10.1002/ajmg.a.20210. Am J Med Genet A. 2003. PMID: 12910486

8

Large-scale medical resequencing for X-linked mental retardation.

Shen Y, Wu BL, Gusella JF. Shen Y, et al. Among authors: wu bl. Clin Chem. 2010 Mar;56(3):339-41. doi: 10.1373/clinchem.2009.135020. Epub 2009 Dec 29. Clin Chem. 2010. PMID: 20040618 No abstract available.

9

Microarray-based genomic DNA profiling technologies in clinical molecular diagnostics.

Shen Y, Wu BL. Shen Y, et al. Among authors: wu bl. Clin Chem. 2009 Apr;55(4):659-69. doi: 10.1373/clinchem.2008.112821. Epub 2009 Feb 20. Clin Chem. 2009. PMID: 19233918 Review.

10

Effectiveness of sequencing connexin 26 (GJB2) in cases of familial or sporadic childhood deafness referred for molecular diagnostic testing.

Wu BL, Lindeman N, Lip V, Adams A, Amato RS, Cox G, Irons M, Kenna M, Korf B, Raisen J, Platt O. Wu BL, et al. Genet Med. 2002 Jul-Aug;4(4):279-88. doi: 10.1097/00125817-200207000-00006. Genet Med. 2002. PMID: 12172394 Free article.

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