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Human Molecular Genetics|December 15, 2000
Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophyS E Wilkie, R J Newbold, E Deery, et al.The American Journal of Emergency Medicine|July 1, 1994
Effectiveness of transnasal butorphanol for the treatment of musculoskeletal painJ L Scott, M S Smith, S M Sanford, et al.Genomics|February 1, 1993
Irradiation hybrids for human chromosome 11: characterization and use for generating region-specific markers in 11q14-q23G T Gillett, C M McConville, P J Byrd, et al.Human Molecular Genetics|June 9, 1998
Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophyR E Kelsell, K Gregory-Evans, A M Payne, et al.Journal of Medical Genetics|November 17, 2007
A novel connexin50 mutation associated with congenital nuclear pulverulent cataractsA Arora, P J Minogue, X Liu, et al.Journal of Evolutionary Biology|May 28, 2015
Visual system evolution and the nature of the ancestral snakeB F Simões, F L Sampaio, C Jared, et al.Human Molecular Genetics|May 20, 1999
N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratodermaL Rickman, D Simrak, H P Stevens, et al.Journal of Medical Genetics|January 7, 2006
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataractA Arora, P J Minogue, X Liu, et al.Nature Genetics|July 11, 2000
Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapyR R Ali, G M Sarra, C Stephens, et al.The New England Journal of Medicine|September 10, 1981
Hemoglobin H disease and mental retardation: a new syndrome or a remarkable coincidence?D J Weatherall, D R Higgs, C Bunch, et al.Pageof 15