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Year Number of Results
2005 1
2007 1
2008 2
2009 1
2010 1
2011 1
2013 1
2014 1
2024 0

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Page 1
Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes.
Qiao Y, Mondal K, Trapani V, Wen J, Carpenter G, Wildin R, Price EM, Gibbons RJ, Eichmeyer J, Jiang R, DuPont B, Martell S, Lewis SM, Robinson WP, O'Driscoll M, Wolf FI, Zwick ME, Rajcan-Separovic E. Qiao Y, et al. Hum Mutat. 2014 Jan;35(1):58-62. doi: 10.1002/humu.22465. Hum Mutat. 2014. PMID: 24130152
Targeted sequencing of the human X chromosome exome.
Mondal K, Shetty AC, Patel V, Cutler DJ, Zwick ME. Mondal K, et al. Genomics. 2011 Oct;98(4):260-5. doi: 10.1016/j.ygeno.2011.04.004. Epub 2011 Apr 16. Genomics. 2011. PMID: 21524701 Free PMC article.
Microarray oligonucleotide probe designer (MOPeD): A web service.
Patel VC, Mondal K, Shetty AC, Horner VL, Bedoyan JK, Martin D, Caspary T, Cutler DJ, Zwick ME. Patel VC, et al. Open Access Bioinformatics. 2010 Nov 1;2(2010):145-155. doi: 10.2147/OAB.S13741. Open Access Bioinformatics. 2010. PMID: 21379402 Free PMC article.
A genome sequencing center in every lab.
Zwick ME. Zwick ME. Eur J Hum Genet. 2005 Nov;13(11):1167-8. doi: 10.1038/sj.ejhg.5201504. Eur J Hum Genet. 2005. PMID: 16251888 No abstract available.