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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 1 |
2010 | 1 |
2013 | 1 |
2014 | 1 |
2015 | 2 |
2018 | 1 |
2020 | 1 |
2024 | 0 |
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7 results
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Page 1
Evaluating rare variants in complex disorders using next-generation sequencing.
Curr Psychiatry Rep. 2013 Apr;15(4):349. doi: 10.1007/s11920-013-0349-4.
Curr Psychiatry Rep. 2013.
PMID: 23435969
Free PMC article.
Review.
Microarray-based mutation detection in the dystrophin gene.
Hegde MR, Chin EL, Mulle JG, Okou DT, Warren ST, Zwick ME.
Hegde MR, et al.
Hum Mutat. 2008 Sep;29(9):1091-9. doi: 10.1002/humu.20831.
Hum Mutat. 2008.
PMID: 18663755
Free PMC article.
Item in Clipboard
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects.
Ramachandran D, Zeng Z, Locke AE, Mulle JG, Bean LJ, Rosser TC, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Feingold E, Sherman SL, Zwick ME.
Ramachandran D, et al.
G3 (Bethesda). 2015 Jul 20;5(10):1961-71. doi: 10.1534/g3.115.019943.
G3 (Bethesda). 2015.
PMID: 26194203
Free PMC article.
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Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
Trevino CE, Holleman AM, Corbitt H, Maslen CL, Rosser TC, Cutler DJ, Johnston HR, Rambo-Martin BL, Oberoi J, Dooley KJ, Capone GT, Reeves RH, Cordell HJ, Keavney BD, Agopian AJ, Goldmuntz E, Gruber PJ, O'Brien JE Jr, Bittel DC, Wadhwa L, Cua CL, Moskowitz IP, Mulle JG, Epstein MP, Sherman SL, Zwick ME.
Trevino CE, et al.
Sci Rep. 2020 Oct 22;10(1):18051. doi: 10.1038/s41598-020-74650-4.
Sci Rep. 2020.
PMID: 33093519
Free PMC article.
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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.
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Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defects.
Ramachandran D, Mulle JG, Locke AE, Bean LJ, Rosser TC, Bose P, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Sherman SL, Zwick ME.
Ramachandran D, et al.
Genet Med. 2015 Jul;17(7):554-60. doi: 10.1038/gim.2014.144. Epub 2014 Oct 23.
Genet Med. 2015.
PMID: 25341113
Free PMC article.
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Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects.
Rambo-Martin BL, Mulle JG, Cutler DJ, Bean LJH, Rosser TC, Dooley KJ, Cua C, Capone G, Maslen CL, Reeves RH, Sherman SL, Zwick ME.
Rambo-Martin BL, et al.
G3 (Bethesda). 2018 Jan 4;8(1):105-111. doi: 10.1534/g3.117.300366.
G3 (Bethesda). 2018.
PMID: 29141989
Free PMC article.
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