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Ophthalmology|July 13, 2000
Ocular histopathologic study of a patient with the T 8993-G point mutation in Leigh's syndromeN Hayashi, M T Geraghty, W R GreenDiabetes & Metabolism|February 8, 2014
A novel heterozygous mutation in the glucokinase gene conferring exercise-induced symptomatic hyperglycaemia responsive to sulfonylureaM S E Ebrahim, M L Lawson, M T GeraghtyGenomics|August 1, 1993
Isolation and characterization of an ornithine aminotransferase-related sequence (OATL3) mapping to 10q26M T Geraghty, W G Kearns, P L Pearson, et al.Journal of Inherited Metabolic Disease|January 14, 1998
A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuriaS Naidu, S R Dlouhy, M T Geraghty, et al.Clinical and Experimental Dermatology|June 15, 2005
Identification of a recurrent mutation in the human hairless gene underlying atrichia with papular lesionsM Massé, A Martinez-Mir, H Lam, et al.The Journal of Biological Chemistry|March 27, 1999
Identification of peroxisomal acyl-CoA thioesterases in yeast and humansJ M Jones, K Nau, M T Geraghty, et al.Human Molecular Genetics|October 1, 1994
Characterization of a cystathionine beta-synthase allele with three mutations in cis in a patient with B6 nonresponsive homocystinuriaM Marble, M T Geraghty, R de Franchis, et al.Journal of Inherited Metabolic Disease|May 9, 2000
Three cases of intravenous sodium benzoate and sodium phenylacetate toxicity occurring in the treatment of acute hyperammonaemiaV Praphanphoj, S A Boyadjiev, L J Waber, et al.Genomics|May 1, 1991
Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short armR G Lafreniere, M T Geraghty, D Valle, et al.Journal of Medical Genetics|April 1, 1988
Linkage analysis of X linked retinitis pigmentosa in the Irish populationG J Farrar, M T Geraghty, J M Moloney, et al.Pageof 5