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Microarray testing in clinical diagnosis: an analysis of 5,300 New Zealand patients.
Mol Cytogenet. 2016 Mar 31;9:29. doi: 10.1186/s13039-016-0237-9. eCollection 2016.
Mol Cytogenet. 2016.
PMID: 27034718
Free PMC article.
Developmental delay referrals and the roles of Fragile X testing and molecular karyotyping: a New Zealand perspective.
Doherty E, O'Connor R, Zhang A, Lim C, Love JM, Ashton F, Claxton K, Gregersen N, George AM, Love DR.
Doherty E, et al. Among authors: claxton k.
Mol Med Rep. 2013 May;7(5):1710-4. doi: 10.3892/mmr.2013.1386. Epub 2013 Mar 20.
Mol Med Rep. 2013.
PMID: 23525284
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SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia.
Nickerson SL, Marquis-Nicholson R, Claxton K, Ashton F, Leong IU, Prosser DO, Love JM, George AM, Taylor G, Wilson C, Gardner RJ, Love DR.
Nickerson SL, et al. Among authors: claxton k.
Microarrays (Basel). 2015 Oct 23;4(4):490-502. doi: 10.3390/microarrays4040490.
Microarrays (Basel). 2015.
PMID: 27600236
Free PMC article.
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