Christopher P Bennett

Christopher P Bennett

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Christopher P Bennett

Christopher P Bennett

Publications by authors named "Christopher P Bennett"

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11Publications

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Early Repolarization Syndrome; Mechanistic Theories and Clinical Correlates.

Front Physiol 2016 30;7:266. Epub 2016 Jun 30.

West Yorkshire Arrhythmia Service, Leeds General InfirmaryLeeds, UK; Regional Inherited Cardiovascular Conditions Service, Leeds General InfirmaryLeeds, UK.

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http://dx.doi.org/10.3389/fphys.2016.00266DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927622PMC
July 2016

Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism.

J Med Genet 2014 Oct 14;51(10):659-68. Epub 2014 Aug 14.

MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.

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http://dx.doi.org/10.1136/jmedgenet-2014-102573DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173748PMC
October 2014

The common TMC1 mutation c.100C>T (p.Arg34X) is not a significant cause of deafness in British Asians.

Genet Test Mol Biomarkers 2012 May 30;16(5):453-5. Epub 2012 Jan 30.

Clinical Genetics, Yorkshire Regional Genetics Service, Leeds, United Kingdom.

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http://dx.doi.org/10.1089/gtmb.2011.0254DOI Listing
May 2012

Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy.

Nat Genet 2008 Jun 25;40(6):789-93. Epub 2008 May 25.

Leeds Institute of Molecular Medicine, University of Leeds, St. James's University Hospital, Beckett Street, Leeds LS9 7TF, UK.

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http://dx.doi.org/10.1038/ng.153DOI Listing
June 2008

A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24.

Hum Genet 2002 Oct 7;111(4-5):456-61. Epub 2002 Sep 7.

Section of Medical and Molecular Genetics, Department of Paediatrics and Child Health, University of Birmingham Medical School, Birmingham, B15 2TT, UK.

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http://dx.doi.org/10.1007/s00439-002-0817-0DOI Listing
October 2002