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Genomics|January 20, 1995
Localization of multiple human dihydrodiol dehydrogenase (DDH1 and DDH2) and chlordecone reductase (CHDR) genes in chromosome 10 by the polymerase chain reaction and fluorescence in situ hybridizationM Khanna, K N Qin, I Klisak, et al.Cancer Genetics and Cytogenetics|May 1, 1990
Use of conditioned media in cell culture can mask cytogenetic abnormalities in acute leukemiaG X Sun, H P Koeffler, R P Gale, et al.Human Genetics|February 15, 1979
Evidence for a null allele at the esterase D (EC 3.1.1.1) locusR S Sparkes, S Targum, E Gershon, et al.Medicine|March 1, 1991
Ataxia-telangiectasia: an interdisciplinary approach to pathogenesisR A Gatti, E Boder, H V Vinters, et al.Science (New York, N.Y.)|June 4, 1976
Direct evidence for a bone marrow origin of the alveolar macrophage in manE D Thomas, R E Ramberg, G E Sale, et al.Current Eye Research|October 1, 1986
Assignment of the rhodopsin gene to human chromosome three, region 3q21-3q24 by in situ hybridization studiesR S Sparkes, I Klisak, D Kaufman, et al.Genetic Epidemiology|January 1, 1990
Genetic epidemiology of bilateral breast cancer: a linkage analysis using the affected-pedigree-member methodR W Haile, A M Goldstein, D E Weeks, et al.Genetic Epidemiology|January 1, 1986
Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group-specific loci: use of restriction fragment length polymorphisms extends exclusion regionK K Kidd, J R Kidd, C M Castiglione, et al.Lancet (London, England)|June 20, 1987
Do oncogenes determine clinical features in chronic myeloid leukaemia?O Dreazen, I Klisak, F Rassool, et al.Journal of Medical Genetics|February 1, 1985
A family with three independent autosomal translocations associated with 7q32----7qter syndromeH N Bass, R S Sparkes, M M Lessner, et al.Pageof 72