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Investigative Ophthalmology & Visual Science|February 1, 1995
mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophyD A Pillers, R G Weleber, W R Woodward, et al.
American Journal of Human Genetics|August 1, 1991
Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girlJ T Clarke, W L Greer, P M Strasberg, et al.
Diseases of the Colon and Rectum|February 1, 1994
Combined use of molecular and biomarkers for presymptomatic carrier risk assessment in familial adenomatous polyposis: implications for screening guidelinesB V Bapat, J A Parker, T Berk, et al.
Human Molecular Genetics|August 13, 1998
Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retinaP L Howard, G Y Dally, M H Wong, et al.
Ophthalmology|October 16, 1999
Isolated sulfite oxidase deficiency: review of two cases in one familyM C Edwards, J L Johnson, B Marriage, et al.
The Journal of Biological Chemistry|October 25, 1990
Cloning and expression of rat histidase. Homology to two bacterial histidases and four phenylalanine ammonia-lyasesR G Taylor, M A Lambert, E Sexsmith, et al.
Muscle & Nerve|January 12, 1999
Dystrophin isoforms DP71 and DP427 have distinct roles in myogenic cellsP L Howard, G Y Dally, S D Ditta, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminusM J Cullen, J Walsh, L V Nicholson, et al.
American Journal of Medical Genetics|August 9, 1996
Tissue-specific methylation differences and cognitive function in fragile X premutation femalesD J Allingham-Hawkins, C A Brown, R Babul, et al.
American Journal of Human Genetics|August 1, 1992
Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosomeJ T Clarke, P J Wilson, C P Morris, et al.
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