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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 2
2004 1
2005 4
2006 3
2007 4
2008 7
2009 7
2010 8
2011 1
2012 6
2013 3
2015 3
2016 3
2017 1
2018 1
2019 1
2021 2
2022 2
2024 0

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59 results

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Page 1
Microdeletion and microduplication syndromes.
Weise A, Mrasek K, Klein E, Mulatinho M, Llerena JC Jr, Hardekopf D, Pekova S, Bhatt S, Kosyakova N, Liehr T. Weise A, et al. Among authors: mrasek k. J Histochem Cytochem. 2012 May;60(5):346-58. doi: 10.1369/0022155412440001. Epub 2012 Mar 6. J Histochem Cytochem. 2012. PMID: 22396478 Free PMC article. Review.
Multicolor FISH methods in current clinical diagnostics.
Liehr T, Weise A, Hamid AB, Fan X, Klein E, Aust N, Othman MA, Mrasek K, Kosyakova N. Liehr T, et al. Among authors: mrasek k. Expert Rev Mol Diagn. 2013 Apr;13(3):251-5. doi: 10.1586/erm.12.146. Expert Rev Mol Diagn. 2013. PMID: 23570403 Review.
Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family.
Wafa A, Ali B, Moassass F, Kheder M, Aljapawe A, Al-Halabi B, Mrasek K, Liehr T, Al-Achkar W. Wafa A, et al. Among authors: mrasek k. Mol Genet Genomic Med. 2022 Feb;10(2):e1854. doi: 10.1002/mgg3.1854. Epub 2022 Jan 15. Mol Genet Genomic Med. 2022. PMID: 35032366 Free PMC article.
Parental origin of deletions and duplications - about the necessity to check for cryptic inversions.
Liehr T, Schreyer I, Kuechler A, Manolakos E, Singer S, Dufke A, Wilhelm K, Jančušková T, Čmejla R, Othman MAK, Al-Rikabi AH, Mrasek K, Ziegler M, Kankel S, Kreskowski K, Weise A. Liehr T, et al. Among authors: mrasek k. Mol Cytogenet. 2018 Mar 9;11:20. doi: 10.1186/s13039-018-0369-1. eCollection 2018. Mol Cytogenet. 2018. PMID: 29541160 Free PMC article.
59 results