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Australian Paediatric Journal|January 1, 1988
Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophyJ C Mulley, A K Gedeon, E A Haan, et al.AJNR. American Journal of Neuroradiology|November 1, 1992
MR of the brain using fluid-attenuated inversion recovery (FLAIR) pulse sequencesB De Coene, J V Hajnal, P Gatehouse, et al.AJR. American Journal of Roentgenology|February 1, 1991
Comparison of iohexol with barium in gastrointestinal studies of infants and childrenM D Cohen, R Towbin, S Baker, et al.The Journal of Pathology|January 18, 2007
Decreased EXT expression and intracellular accumulation of heparan sulphate proteoglycan in osteochondromas and peripheral chondrosarcomasL Hameetman, G David, A Yavas, et al.Neuroreport|July 4, 2001
MRI changes in multiple sclerosis following treatment with lofepramine and L-phenylalanineB K Puri, G M Bydder, K R Chaudhuri, et al.Diabetes|December 2, 1999
ATP-sensitive potassium channels and efaroxan-induced insulin release in the electrofusion-derived BRIN-BD11 beta-cell lineJ C Chapman, N H McClenaghan, K E Cosgrove, et al.Cytogenetic and Genome Research|March 17, 2009
Methods to detect CNVs in the human genomeE Aten, S J White, M E Kalf, et al.American Journal of Human Genetics|March 1, 1992
Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome IN G Laing, B T Majda, P A Akkari, et al.Electrophoresis|March 1, 1997
Electrophoretic analysis of the novel antigen for the gastrointestinal-specific monoclonal antibody, A33H Ji, R L Moritz, G E Reid, et al.Journal of Medical Genetics|April 3, 2004
Genomic imbalances in mental retardationM Kriek, S J White, M C Bouma, et al.Pageof 14