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Prenatal Diagnosis|November 1, 1994
Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective studyD H Spathas, A Divane, G M Maniatis, et al.
Journal of Medical Genetics|September 1, 1987
Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-ablJ M Connor, L A Pirrit, J R Yates, et al.
British Medical Journal|May 29, 1971
Chromosome breakage and ultrasoundE Boyd, U Abdulla, I Donald, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1982
Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridizationS Malcolm, P Barton, C Murphy, et al.
Cytometry|January 1, 1990
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blotsN P Carter, M E Ferguson-Smith, N A Affara, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|June 17, 2006
Effect of resistance training on risk of coronary artery disease in women with multiple sclerosisL J White, S C McCoy, V Castellano, et al.
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