Paul Rutland

Paul Rutland

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Paul Rutland

Paul Rutland

Publications by authors named "Paul Rutland"

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Genomic Insights into Cardiomyopathies: A Comparative Cross-Species Review.

Vet Sci 2017 Mar 21;4(1). Epub 2017 Mar 21.

Faculty of Medicine and Health Sciences, School of Veterinary Medicine and Science, The University of Nottingham, Sutton Bonington Campus, Loughborough LE12 5RD, UK.

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http://dx.doi.org/10.3390/vetsci4010019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606618PMC
March 2017

Mitochondrial m.1584A 12S m62A rRNA methylation in families with m.1555A>G associated hearing loss.

Hum Mol Genet 2015 Feb 9;24(4):1036-44. Epub 2014 Oct 9.

Genetics and Genomic Medicine, UCL Institute of Child Health, London WC1N 1EH, UK, Centre for Auditory Research, UCL Ear Institute, London WC1X 8EE, UK

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http://dx.doi.org/10.1093/hmg/ddu518DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986548PMC
February 2015

First report of Mycobacterium bovis DNA in human remains from the Iron Age.

Microbiology 2007 Apr;153(Pt 4):1243-9

Centre for Molecular Microbiology and Infectious Diseases, Imperial College of Science, Technology and Medicine, London, UK.

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http://mic.microbiologyresearch.org/content/journal/micro/10
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http://dx.doi.org/10.1099/mic.0.2006/002154-0DOI Listing
April 2007

Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination.

Neurogenetics 2007 Jan 13;8(1):39-44. Epub 2006 Sep 13.

Clinical and Molecular Genetics Unit, Institute of Child Health, London, UK.

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http://dx.doi.org/10.1007/s10048-006-0062-0DOI Listing
January 2007

A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.

Am J Med Genet B Neuropsychiatr Genet 2006 Mar;141B(2):184-91

Developmental Biology Unit, Institute of Child Health and Great Ormond Street Hospital for Children NHS Trust, University College London, London, United Kingdom.

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http://dx.doi.org/10.1002/ajmg.b.30237DOI Listing
March 2006

Kantaputra mesomelic dysplasia: a second reported family.

Am J Med Genet A 2004 Jul;128A(1):6-11

Clinical and Molecular Genetics Unit, Institute of Child Health, 30 Guilford Street, London WC1N 3EH, United Kingdom.

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http://dx.doi.org/10.1002/ajmg.a.20640DOI Listing
July 2004