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Cytogenetic and Genome Research|November 15, 2007
Familial cancer syndromes: catalog with commentsF HechtAmerican Journal of Human Genetics|January 1, 1983
The combined effects of FUdR addition and methionine depletion on the X-chromosome fragile siteT W Glover, P N Howard-PeeblesAmerican Journal of Medical Genetics|September 15, 1991
Severe anomalies associated with ring chromosome 7L G Biesecker, B Cox, T W GloverCancer Genetics and Cytogenetics|January 1, 1986
Fragile sites: overview, occurrence in acute nonlymphocytic leukemia and effects of caffeine on expressionT W Glover, J Coyle-Morris, R MorganGene|November 25, 1997
A phosphoglycerate mutase brain isoform (PGAM 1) pseudogene is localized within the human Menkes disease gene (ATP7 A)H A Dierick, J F Mercer, T W GloverCytogenetics and Cell Genetics|January 1, 1989
A somatic cell hybrid panel to facilitate identification of DNA sequences in the vicinity of the incontinentia pigmenti locus (IP1)J L Gorski, C K Stein, T W GloverHuman Genetics|January 1, 1984
DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomesT W Glover, C Berger, J Coyle, et al.American Journal of Medical Genetics|December 1, 1990
A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndromeJ L Gorski, W R Uhlmann, T W GloverCytogenetics and Cell Genetics|July 25, 1998
Y;16 translocation breakpoint associated with a partial Turner phenotype identifies a foamy virus insertionS Schmidt Drury, R P Erickson, T W GloverPageof 22