Zhang VW - Search Results

1

A Comprehensive Strategy for Accurate Mutation Detection of the Highly Homologous PMS2.

Li J, Dai H, Feng Y, Tang J, Chen S, Tian X, Gorman E, Schmitt ES, Hansen TA, Wang J, Plon SE, Zhang VW, Wong LJ. Li J, et al. Among authors: zhang vw. J Mol Diagn. 2015 Sep;17(5):545-53. doi: 10.1016/j.jmoldx.2015.04.001. J Mol Diagn. 2015. PMID: 26320870 Free article.

2

Determination of the clinical significance of an unclassified variant.

Zhang VW, Wang J. Zhang VW, et al. Methods Mol Biol. 2012;837:337-48. doi: 10.1007/978-1-61779-504-6_23. Methods Mol Biol. 2012. PMID: 22215559

3

An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory's experience.

Wang J, Schmitt ES, Landsverk ML, Zhang VW, Li FY, Graham BH, Craigen WJ, Wong LJ. Wang J, et al. Among authors: zhang vw. Genet Med. 2012 Jun;14(6):620-6. doi: 10.1038/gim.2012.4. Epub 2012 Mar 8. Genet Med. 2012. PMID: 22402757 Free article.

4

Diagnostic approaches to apparent homozygosity.

Landsverk ML, Douglas GV, Tang S, Zhang VW, Wang GL, Wang J, Wong LJ. Landsverk ML, et al. Among authors: zhang vw. Genet Med. 2012 Oct;14(10):877-82. doi: 10.1038/gim.2012.58. Epub 2012 May 17. Genet Med. 2012. PMID: 22595940 Free article.

5

Mitochondrial myopathy due to novel missense mutation in the cytochrome c oxidase 1 gene.

Massie R, Wang J, Chen LC, Zhang VW, Collins MP, Wong LJ, Milone M. Massie R, et al. Among authors: zhang vw. J Neurol Sci. 2012 Aug 15;319(1-2):158-63. doi: 10.1016/j.jns.2012.05.003. Epub 2012 May 24. J Neurol Sci. 2012. PMID: 22632780

6

Clinical application of massively parallel sequencing in the molecular diagnosis of glycogen storage diseases of genetically heterogeneous origin.

Wang J, Cui H, Lee NC, Hwu WL, Chien YH, Craigen WJ, Wong LJ, Zhang VW. Wang J, et al. Among authors: zhang vw. Genet Med. 2013 Feb;15(2):106-14. doi: 10.1038/gim.2012.104. Epub 2012 Aug 16. Genet Med. 2013. PMID: 22899091 Free article.

7

Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects.

Tang S, Wang J, Zhang VW, Li FY, Landsverk M, Cui H, Truong CK, Wang G, Chen LC, Graham B, Scaglia F, Schmitt ES, Craigen WJ, Wong LJ. Tang S, et al. Among authors: zhang vw. Hum Mutat. 2013 Jun;34(6):882-93. doi: 10.1002/humu.22307. Epub 2013 Apr 2. Hum Mutat. 2013. PMID: 23463613

8

Biochemical, molecular, and clinical diagnoses of patients with cerebral creatine deficiency syndromes.

Comeaux MS, Wang J, Wang G, Kleppe S, Zhang VW, Schmitt ES, Craigen WJ, Renaud D, Sun Q, Wong LJ. Comeaux MS, et al. Among authors: zhang vw. Mol Genet Metab. 2013 Jul;109(3):260-8. doi: 10.1016/j.ymgme.2013.04.006. Epub 2013 Apr 17. Mol Genet Metab. 2013. PMID: 23660394

9

Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene.

Chanprasert S, Wang J, Weng SW, Enns GM, Boué DR, Wong BL, Mendell JR, Perry DA, Sahenk Z, Craigen WJ, Alcala FJ, Pascual JM, Melancon S, Zhang VW, Scaglia F, Wong LJ. Chanprasert S, et al. Among authors: zhang vw. Mol Genet Metab. 2013 Sep-Oct;110(1-2):153-61. doi: 10.1016/j.ymgme.2013.07.009. Epub 2013 Jul 17. Mol Genet Metab. 2013. PMID: 23932787

10

Improved molecular diagnosis by the detection of exonic deletions with target gene capture and deep sequencing.

Feng Y, Chen D, Wang GL, Zhang VW, Wong LJ. Feng Y, et al. Among authors: zhang vw. Genet Med. 2015 Feb;17(2):99-107. doi: 10.1038/gim.2014.80. Epub 2014 Jul 17. Genet Med. 2015. PMID: 25032985 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

112 results

Search Page

Filters