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Somatic Cell Genetics|September 1, 1977
Genetics of the mammalian phenylalanine hydroxylase system: I. Isolation of phenylalanine hydroxylase-deficient tyrosine auxotrophs from rat hepatoma cellsK H Choo, R G CottonThe Biochemical Journal|January 1, 1981
Double-label reductive methylation of tissue proteins for precision two-dimensional polyacrylamide-gel electrophoretic analysisJ M Finger, K H ChooBiochemical Genetics|October 1, 1979
Genetics of the mammalian phenylalanine hydroxylase system. II. Immunological and two-dimensional gel electrophoretic studies of phenylalanine hydroxylase in cultured normal and mutant rat hepatoma cellsK H Choo, R G CottonProceedings of the National Academy of Sciences of the United States of America|September 1, 1993
Targeting and germ-line transmission of a null mutation at the metallothionein I and II loci in mouseA E Michalska, K H ChooJournal of Inherited Metabolic Disease|January 1, 1992
Comparison of total cellular DNA, mRNA, and rRNA levels between normals and Down syndrome patientsC I McQuillan, K H ChooGenomics|August 1, 1989
Evolution of alpha-satellite DNA on human acrocentric chromosomesK H Choo, B Vissel, E EarleNucleic Acids Research|October 11, 1990
A homologous subfamily of satellite III DNA on human chromosomes 14 and 22K H Choo, E Earle, C McQuillanCytogenetics and Cell Genetics|January 1, 1992
A satellite III sequence shared by human chromosomes 13, 14, and 21 that is contiguous with alpha satellite DNAB Vissel, A Nagy, K H ChooHuman Genetics|May 1, 1989
Amplification of satellite III DNA in an unusually large chromosome 14p+ variantE Earle, S Dale, K H ChooAmerican Journal of Human Genetics|October 1, 1988
Application of DNA-DNA hybridization of dual labeled probes to the detection of trisomy 21, monosomy 21, and sex determinationH H Dahl, K H Choo, D M DanksPageof 205