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Molecular and Cellular Biology|January 1, 1990
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy geneH J Klamut, S B Gangopadhyay, R G Worton, et al.
American Journal of Medical Genetics|May 30, 1998
FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndromeK Chun, J Siegel-Bartelt, D Chitayat, et al.
The EMBO Journal|December 1, 1991
Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophyS E Bodrug, J J Holden, P N Ray, et al.
Genomics|March 1, 1993
Identification and partial characterization of a candidate gene for X-linked retinopathies using a lateral approachP Wong, I M MacDonald, R Sood, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 1, 1989
Corneal toxic changes after cataract extractionR W Zabel, G Mintsioulis, I M MacDonald, et al.
The Medical Journal of Australia|March 15, 1975
Changing concepts in the management of hypertensionP Kincaid-Smith, I M Macdonald, A Hua, et al.
Nucleic Acids Research|April 15, 1997
A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifsH J Klamut, L O Bosnoyan-Collins, R G Worton, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|October 1, 1995
Effect of retinoic acid on expression of transforming growth factor-beta by retinal pigment epithelial cells in cultureI M MacDonald, R Pannu, K Kovithavongs, et al.
Transplantation|December 1, 1988
Adverse influence of recipient lymphoid resistance to in vitro immunosuppression on the outcome of kidney transplantsD M Francis, L J Dumble, L Bowes, et al.
American Journal of Medical Genetics|January 1, 1991
Autosomal recessive inheritance of vasopressin-resistant diabetes insipidusJ M Langley, J W Balfe, T Selander, et al.
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