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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
Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing.
Field M, Dudding-Byth T, Arpone M, Baker EK, Aliaga SM, Rogers C, Hickerton C, Francis D, Phelan DG, Palmer EE, Amor DJ, Slater H, Bretherton L, Ling L, Godler DE. Field M, et al. Among authors: slater h. Int J Mol Sci. 2019 Aug 11;20(16):3907. doi: 10.3390/ijms20163907. Int J Mol Sci. 2019. PMID: 31405222 Free PMC article.
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.
Baker EK, Arpone M, Aliaga SM, Bretherton L, Kraan CM, Bui M, Slater HR, Ling L, Francis D, Hunter MF, Elliott J, Rogers C, Field M, Cohen J, Cornish K, Santa Maria L, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE. Baker EK, et al. Among authors: slater hr. Mol Autism. 2019 May 3;10:21. doi: 10.1186/s13229-019-0271-7. eCollection 2019. Mol Autism. 2019. PMID: 31073396 Free PMC article.
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
Use of ubiquitous, highly heterozygous copy number variants and digital droplet polymerase chain reaction to monitor chimerism after allogeneic haematopoietic stem cell transplantation.
Whitlam JB, Ling L, Swain M, Harrington T, Mirochnik O, Brooks I, Cronin S, Challis J, Petrovic V, Bruno DL, Mechinaud F, Conyers R, Slater H. Whitlam JB, et al. Among authors: slater h. Exp Hematol. 2017 May;49:39-47.e5. doi: 10.1016/j.exphem.2017.01.004. Epub 2017 Jan 29. Exp Hematol. 2017. PMID: 28147232 Free article.
Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia.
Hwang YT, Dudding T, Aliaga SM, Arpone M, Francis D, Li X, Slater HR, Rogers C, Bretherton L, du Sart D, Heard R, Godler DE. Hwang YT, et al. Among authors: slater hr. Genes (Basel). 2016 Sep 21;7(9):68. doi: 10.3390/genes7090068. Genes (Basel). 2016. PMID: 27657133 Free PMC article.
59 results