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Arthritis and Rheumatism|January 1, 1987
Linkage studies of HLA and rheumatoid arthritis in multicase familiesD J Walker, J Burn, I D Griffiths, et al.American Journal of Physical Anthropology|December 5, 1997
The founding mitochondrial DNA lineages of Tristan da Cunha IslandersH Soodyall, T Jenkins, A Mukherjee, et al.Annals of the Rheumatic Diseases|November 1, 1992
P blood group phenotype, proteus antibody titres, and rheumatoid arthritisC M Deighton, J Gray, D F Roberts, et al.Clinical Genetics|April 1, 1983
Reflections on muscular dystrophy in a Sudanese kindredM A Salih, D F Roberts, M I Omer, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|March 26, 1998
Clinical features in affected individuals from 21 pedigrees with dominant optic atrophyM Votruba, F W Fitzke, G E Holder, et al.Human Mutation|March 29, 2000
Novel mutations of the RPGR gene in RP3 familiesI Zito, M B Gorin, C Plant, et al.Genomics|October 1, 1992
The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13)M E Porteous, A Curtis, S Lindsay, et al.Journal of Medical Genetics|June 1, 1996
A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17pE E Tarttelin, C Plant, J Weissenbach, et al.European Journal of Human Genetics : EJHG|October 20, 2000
NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophiesD A Bessant, A M Payne, C Plant, et al.Human Molecular Genetics|January 1, 1997
A locus for autosomal dominant posterior polar cataract on chromosome 1pA C Ionides, V Berry, D S Mackay, et al.Pageof 37