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Page 1
A second locus for Aicardi-Goutieres syndrome at chromosome 13q14-21.
J Med Genet. 2006 May;43(5):444-50. doi: 10.1136/jmg.2005.031880. Epub 2005 May 20.
J Med Genet. 2006.
PMID: 15908569
Free PMC article.
Continuing professional development: putting the learner back at the centre.
Macdougall C, Epstein M, Highet L.
Macdougall C, et al. Among authors: highet l.
Arch Dis Child Educ Pract Ed. 2017 Oct;102(5):249-253. doi: 10.1136/archdischild-2016-310864. Epub 2017 Mar 16.
Arch Dis Child Educ Pract Ed. 2017.
PMID: 28302733
Item in Clipboard
Variable phenotype including Leigh syndrome with a 9185T>C mutation in the MTATP6 gene.
Childs AM, Hutchin T, Pysden K, Highet L, Bamford J, Livingston J, Crow YJ.
Childs AM, et al. Among authors: highet l.
Neuropediatrics. 2007 Dec;38(6):313-6. doi: 10.1055/s-2008-1065355.
Neuropediatrics. 2007.
PMID: 18461509
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Using ePortfolios to support clinical training in paediatrics.
Morris AP, Highet LJ, Frazer SE.
Morris AP, et al. Among authors: highet lj.
Arch Dis Child Educ Pract Ed. 2010 Oct;95(5):157-64. doi: 10.1136/adc.2008.142265. Epub 2010 Jul 30.
Arch Dis Child Educ Pract Ed. 2010.
PMID: 20675525
No abstract available.
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Characterization of the human Xq21.3/Yp11 homology block and conservation of organization in primates.
Sargent CA, Boucher CA, Blanco P, Chalmers IJ, Highet L, Hall N, Ross N, Crow T, Affara NA.
Sargent CA, et al. Among authors: highet l.
Genomics. 2001 Apr 1;73(1):77-85. doi: 10.1006/geno.2000.6491.
Genomics. 2001.
PMID: 11352568
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