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

Year Number of Results
1998 1
1999 2
2000 2
2001 3
2002 1
2003 2
2004 5
2005 2
2006 1
2007 4
2008 6
2009 4
2010 2
2011 5
2012 2
2013 2
2014 2
2015 2
2016 2
2024 0

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45 results

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Page 1
MT-CYB mutations in hypertrophic cardiomyopathy.
Hagen CM, Aidt FH, Havndrup O, Hedley PL, Jespersgaard C, Jensen M, Kanters JK, Moolman-Smook JC, Møller DV, Bundgaard H, Christiansen M. Hagen CM, et al. Among authors: moolman smook jc. Mol Genet Genomic Med. 2013 May;1(1):54-65. doi: 10.1002/mgg3.5. Epub 2013 Apr 12. Mol Genet Genomic Med. 2013. PMID: 24498601 Free PMC article.
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1.
de Villiers CP, van der Merwe L, Crotti L, Goosen A, George AL Jr, Schwartz PJ, Brink PA, Moolman-Smook JC, Corfield VA. de Villiers CP, et al. Among authors: moolman smook jc. Circ Cardiovasc Genet. 2014 Oct;7(5):599-606. doi: 10.1161/CIRCGENETICS.113.000580. Epub 2014 Aug 2. Circ Cardiovasc Genet. 2014. PMID: 25087618 Free PMC article.
Gender in obsessive-compulsive disorder: clinical and genetic findings.
Lochner C, Hemmings SM, Kinnear CJ, Moolman-Smook JC, Corfield VA, Knowles JA, Niehaus DJ, Stein DJ. Lochner C, et al. Among authors: moolman smook jc. Eur Neuropsychopharmacol. 2004 Mar;14(2):105-13. doi: 10.1016/S0924-977X(03)00063-4. Eur Neuropsychopharmacol. 2004. PMID: 15013025 Corrected and republished.
45 results