D. Mechan

Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis.

David Baty, A. Kwiatkowski, D. Mechan et al. · Journal of Clinical Pathology · 1998 · 32 citations · Full text

Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex

Marta García, J.L. Santiago, Anna Terrón et al. · British Journal of Dermatology · 2011 · 29 citations

Chromosomal changes in colorectal adenomas: Relationship to gene mutations and potential for clinical utility

A Leslie, Arlene Stewart, David Baty et al. · Genes Chromosomes and Cancer · 2005 · 29 citations

Delayed diagnosis of oculopharyngeal muscular dystrophy in Scotland: Figure 1

Pankaj Kumar Agarwal, David Mansfield, D. Mechan et al. · British Journal of Ophthalmology · 2011 · 22 citations

Two cases of oculopharyngeal muscular dystrophy (OPMD) with the rare PABPN1 c.35G > C; p.Gly12Ala point mutation

David Robinson, David Hilton‐Jones, David Mansfield et al. · Neuromuscular Disorders · 2011 · 12 citations