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The British Journal of Ophthalmology|April 1, 1993
Clinical features of affected males with X linked ocular albinismS J Charles, J S Green, J W Grant, et al.Journal of Physics. Condensed Matter : an Institute of Physics Journal|October 31, 2013
Oxygen K-edge electron energy loss spectra of hydrous and anhydrous compoundsB Winkler, M Avalos-Borja, V Milman, et al.European Journal of Human Genetics : EJHG|November 26, 1999
Stickler syndrome: further mutations in COL11A1 and evidence for additional locus heterogeneityS Martin, A J Richards, J R Yates, et al.Journal of Medical Genetics|September 1, 1987
Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-ablJ M Connor, L A Pirrit, J R Yates, et al.Journal of Medical Genetics|November 14, 1997
Instability of normal (CTG)n alleles in the DM kinase geneD J Dow, D C Rubinsztein, J R Yates, et al.Human Genetics|July 8, 1999
Exclusion of RAI2 as the causative gene for Nance-Horan syndromeS M Walpole, N Ronce, C Grayson, et al.Neuromuscular Disorders : NMD|July 10, 1999
A protein truncation test for Emery-Dreifuss muscular dystrophy (EMD): detection of N-terminal truncating mutationsP A de Koning Gans, I Ginjaar, E Bakker, et al.Human Genetics|January 1, 1985
Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophyD E Wilcox, N A Affara, J R Yates, et al.The British Journal of Ophthalmology|July 1, 1994
Carrier detection in X linked ocular albinism using linked DNA polymorphismsS J Charles, A T Moore, Y Zhang, et al.Genes & Development|December 4, 2001
The yeast SAS (something about silencing) protein complex contains a MYST-type putative acetyltransferase and functions with chromatin assembly factor ASF1S Osada, A Sutton, N Muster, et al.Pageof 27