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Ophthalmic Genetics|June 1, 1996
Mutation analysis in Canadian families with choroideremiaN Nesslinger, G Mitchell, P Strasberg, et al.Clinical Chemistry|July 1, 1989
Evaluation of the biotinylated (Blugene) vs 32P-labeled cDNA probes of beta-glucocerebrosidase: relative sensitivities in genomic and other systemsP StrasbergBiochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|May 1, 1986
Cerebrosides and psychosine disrupt mitochondrial functionsP StrasbergInternational Journal of Nursing Studies|April 8, 2000
Hunting for Heidegger: questioning the sources in the Benner/Cash debateS HorrocksJournal of Medical Genetics|October 1, 1996
X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindredJ J MacKenzie, J Fitzpatrick, P Babyn, et al.Lipids|December 1, 1992
Increased globotriaosylceramide in familial dysautonomiaP Strasberg, H Yeger, I WarrenClinical and Investigative Medicine. Medecine Clinique Et Experimentale|October 1, 1994
Molecular genetics of inherited eye disordersI M MacDonald, R SasiPalliative Medicine|October 17, 2002
Do children with non-malignant life-threatening conditions receive effective palliative care? A pragmatic evaluation of a local serviceS Horrocks, M Somerset, C SalisburyOphthalmic Genetics|April 26, 2000
Summary of heritable ocular disorders and selected systemic conditions with eye findingsI M MacDonald, D Y MahHuman Genetics|January 1, 1985
Inversion of chromosome 2 (p11p13): frequency and implications for genetic counsellingI M MacDonald, D M CoxPageof 14