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Nature|December 19, 1985
Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophyP N Ray, B Belfall, C Duff, et al.JAMA|April 20, 1994
Health care for black and poor hospitalized Medicare patientsK L Kahn, M L Pearson, E R Harrison, et al.Therapeutic Drug Monitoring|October 1, 1996
Totally automated analysis by robotized PrepStation and liquid chromatography: direct-sample analysis of felbamateS H Wong, E A Sasse, J M Schroeder, et al.Nature|June 2, 1988
The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscleE E Zubrzycka-Gaarn, D E Bulman, G Karpati, et al.Ophthalmology|May 1, 1994
Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophyD A Sigesmund, R G Weleber, D A Pillers, et al.Science (New York, N.Y.)|November 4, 1988
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophyS B Malhotra, K A Hart, H J Klamut, et al.American Journal of Human Genetics|August 1, 1992
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qterC Wijmenga, L A Sandkuijl, P Moerer, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndromeD A Pillers, W K Seltzer, B R Powell, et al.Human Molecular Genetics|December 26, 2001
Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1R Weksberg, J Nishikawa, O Caluseriu, et al.Clinical Genetics|August 8, 2008
The clinical and genetic epidemiology of neuronal ceroid lipofuscinosis in NewfoundlandS J Moore, D J Buckley, A MacMillan, et al.Pageof 13