Showing results (21-30 of 53) with videos related to
Sort By:
Pageof 6
American Journal of Optometry and Physiological Optics|May 1, 1985
Tinted hydrogel lenses permanency of tintF G Lutzi, B R Chou, D J EganAmerican Journal of Human Genetics|March 31, 2000
A novel X-linked dominant condition: X-linked congenital isolated ptosisT F McMullan, A R Collins, A G Tyers, et al.American Journal of Optometry and Physiological Optics|June 1, 1986
Contact lens surface changes after exposure to surfactant and abrasive cleaning proceduresG B Doell, D L Palombi, D J Egan, et al.Leukemia|October 12, 1999
Identification of false-positive CBFbeta/MYH11 RT-PCR resultsS M Hackwell, D O Robinson, J F Harvey, et al.Archives of Medical Research|April 18, 2000
Functional Xp disomy and hypomelanosis of ItoH Rivera, L S Correa-Cerro, D O Robinson, et al.Human Genetics|January 1, 1995
Fluorescence in situ hybridisation studies provide evidence for somatic mosaicism in de novo dystrophin gene deletionsD J Bunyan, J A Crolla, A L Collins, et al.Scandinavian Journal of Gastroenterology|January 1, 1977
Pancreatitis and renal diseaseD O Robinson, M H Alp, A K Grant, et al.Journal of Medical Genetics|May 2, 2006
Oculopharyngeal muscular dystrophy: a point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutationD O Robinson, A J Wills, S R Hammans, et al.Clinical Genetics|January 23, 1999
Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitusR J Gardner, D O Robinson, L Lamont, et al.Genetical Research|October 1, 1990
The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysisD O Robinson, Y Boyd, D Cockburn, et al.Pageof 6