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Clinical Genetics|October 1, 1980
The use of sequential silver and quinacrine staining to determine the parental origin and breakpoints of a ring-22 human chromosomeG Fowler, B Kaiser-McCaw, F HechtThe New England Journal of Medicine|January 9, 1975
Parthenogenic origin of benign ovarian teratomasD Linder, B K McCaw, F HechtAmerican Journal of Medical Genetics|August 1, 1989
Three additional cases of the congenital hypothalamic "hamartoblastoma" (Pallister-Hall) syndromeP D Pallister, F Hecht, J HerrmanAmerican Journal of Medical Genetics|June 1, 1985
Enhanced expression of chromosome fragile site 10q25 in chronic myelogenous leukemiaR Morgan, S S Morgan, F HechtCancer Genetics and Cytogenetics|January 1, 1990
A guide to fragile sites on human chromosomesF Hecht, K H Ramesh, D H LockwoodCancer Genetics and Cytogenetics|January 15, 1985
Nonreciprocal chromosome translocation t(5;14) in cancers of the kidney: adenocarcinoma of the renal parenchyma and transitional cell carcinoma of the kidney pelvisF Hecht, C S Berger, A A SandbergScience (New York, N.Y.)|October 2, 1970
Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in manR E Magenis, F Hecht, E W LovrienJournal of Biomechanical Engineering|February 1, 1992
Numerical simulation of steady flow in a model of the aortic bifurcationM Thiriet, C Pares, E Saltel, et al.Mikrochimica Acta|October 11, 2012
[Electrophoresis of rare earth elements on cellulose acetate]K Aitzetmüller, K Buchtela, F Grass, et al.American Journal of Medical Genetics|March 1, 1988
Deletion mapping of the beta-glucuronidase geneJ E Allanson, R M Gemmill, B K Hecht, et al.Pageof 14