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

Year Number of Results
2002 1
2003 1
2004 3
2005 8
2006 3
2008 3
2009 5
2010 5
2011 4
2012 3
2013 7
2014 6
2015 5
2016 4
2017 3
2018 3
2019 3
2024 0

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59 results

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Page 1
ADGRV1 is implicated in myoclonic epilepsy.
Myers KA, Nasioulas S, Boys A, McMahon JM, Slater H, Lockhart P, Sart DD, Scheffer IE. Myers KA, et al. Among authors: slater h. Epilepsia. 2018 Feb;59(2):381-388. doi: 10.1111/epi.13980. Epub 2017 Dec 20. Epilepsia. 2018. PMID: 29266188
Centric fission--simple and complex mechanisms.
Perry J, Slater HR, Choo KH. Perry J, et al. Among authors: slater hr. Chromosome Res. 2004;12(6):627-40. doi: 10.1023/B:CHRO.0000036594.38997.59. Chromosome Res. 2004. PMID: 15289668 Review.
Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature.
Béna F, Bruno DL, Eriksson M, van Ravenswaaij-Arts C, Stark Z, Dijkhuizen T, Gerkes E, Gimelli S, Ganesamoorthy D, Thuresson AC, Labalme A, Till M, Bilan F, Pasquier L, Kitzis A, Dubourgm C, Rossi M, Bottani A, Gagnebin M, Sanlaville D, Gilbert-Dussardier B, Guipponi M, van Haeringen A, Kriek M, Ruivenkamp C, Antonarakis SE, Anderlid BM, Slater HR, Schoumans J. Béna F, et al. Among authors: slater hr. Am J Med Genet B Neuropsychiatr Genet. 2013 Jun;162B(4):388-403. doi: 10.1002/ajmg.b.32148. Epub 2013 Mar 26. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23533028 Review.
Human centromere repositioning "in progress".
Amor DJ, Bentley K, Ryan J, Perry J, Wong L, Slater H, Choo KH. Amor DJ, et al. Among authors: slater h. Proc Natl Acad Sci U S A. 2004 Apr 27;101(17):6542-7. doi: 10.1073/pnas.0308637101. Epub 2004 Apr 14. Proc Natl Acad Sci U S A. 2004. PMID: 15084747 Free PMC article.
High resolution chromosomal microarray in undiagnosed neurological disorders.
Howell KB, Kornberg AJ, Harvey AS, Ryan MM, Mackay MT, Freeman JL, Rodriguez Casero MV, Collins KJ, Hayman M, Mohamed A, Ware TL, Clark D, Bruno DL, Burgess T, Slater H, McGillivray G, Leventer RJ. Howell KB, et al. Among authors: slater h. J Paediatr Child Health. 2013 Sep;49(9):716-24. doi: 10.1111/jpc.12256. Epub 2013 Jun 3. J Paediatr Child Health. 2013. PMID: 23731025 Clinical Trial.
Use of copy number deletion polymorphisms to assess DNA chimerism.
Bruno DL, Ganesamoorthy D, Thorne NP, Ling L, Bahlo M, Forrest S, Veenendaal M, Katerelos M, Skene A, Ierino FL, Power DA, Slater HR. Bruno DL, et al. Among authors: slater hr. Clin Chem. 2014 Aug;60(8):1105-14. doi: 10.1373/clinchem.2013.216077. Epub 2014 Jun 4. Clin Chem. 2014. PMID: 24899692
59 results