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American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)A Snarey, S Thomas, M C Schneider, et al.Lancet (London, England)|October 7, 1989
Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic diseaseJ Lamb, A O Wilkie, P C Harris, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Construction of a map of chromosome 16 by using radiation hybridsI Ceccherini, G Romeo, S Lawrence, et al.American Journal of Human Genetics|June 1, 1990
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3A O Wilkie, V J Buckle, P C Harris, et al.Human Molecular Genetics|August 1, 1994
Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndromeH H Lemmink, T Mochizuki, L P van den Heuvel, et al.Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|August 18, 2016
A review of the application of autologous blood transfusionJ ZhouZhonghua Bing Li Xue Za Zhi = Chinese Journal of Pathology|June 1, 1989
[Human pituitary growth hormone cell adenomas, ultrastructural and immunoelectron microscopical study]X J ZhouZhonghua Zhong Liu Za Zhi [Chinese Journal of Oncology]|July 1, 1989
[Tumor-associated macrophages in tumor neovascularization--in situ ultrastructural cytochemical and quantitative study]X J ZhouThe Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 5, 2001
A critical role of the strychnine-sensitive glycinergic system in spontaneous retinal waves of the developing rabbitZ J ZhouPageof 367