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Genomics|December 1, 1993
A somatic cell hybrid map of human chromosome 13S S Washington, A M Bowcock, S Gerken, et al.American Journal of Human Genetics|December 1, 1991
Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26)T H Huang, J F Hejtmancik, A Edwards, et al.Human Genetics|January 1, 1996
A clinical and molecular study of mosaicism for trisomy 17L G Shaffer, C McCaskill, J H Hersh, et al.American Journal of Human Genetics|December 1, 1993
Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18R Mewar, A D Kline, W Harrison, et al.Cancer Research|March 4, 2025
A Critical Appraisal of the Utility of Targeting Therapy-Induced Senescence for Cancer TreatmentTareq Saleh, Edward F Greenberg, Anthony C Faber, et al.Bioorganic & Medicinal Chemistry Letters|February 22, 2011
Discovery of histone deacetylase 8 selective inhibitorsWeiping Tang, Tuoping Luo, Edward F Greenberg, et al.Human Genetics|July 1, 1991
Molecular characterization of a patient with del(1)(q23-q25)B Franco, L W Lai, D Patterson, et al.Human Genetics|May 1, 1987
Prenatal diagnosis of cystic fibrosis using linked DNA markers and microvillar intestinal enzyme analysisJ E Spence, G J Buffone, C L Rosenbloom, et al.Journal of Neurogenetics|December 1, 1985
Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophyL H Yamaoka, R J Bartlett, D A Ross, et al.Prenatal Diagnosis|May 1, 1992
Cytogenetic results from the U.S. Collaborative Study on CVSD H Ledbetter, J M Zachary, J L Simpson, et al.Pageof 33