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Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Carrier detection and prenatal diagnosis by intron 22 inversion analysis of the factor VIII geneC Ononye, P V Jenkins, E Goldman, et al.Genomics|September 1, 1995
Detection of steroid 21-hydroxylase alleles using gene-specific PCR and a multiplexed ligation detection reactionD J Day, P W Speiser, P C White, et al.Endocrine Research|February 24, 2001
Regulation of human CYP11B2 and CYP11B1: comparing the role of the common CRE/Ad1 elementM H Bassett, Y Zhang, P C White, et al.American Journal of Human Genetics|October 1, 1986
Frequent deletion and duplication of the steroid 21-hydroxylase genesJ W Werkmeister, M I New, B Dupont, et al.Genomics|September 1, 1995
Gene structure and chromosomal localization of the human HSD11K gene encoding the kidney (type 2) isozyme of 11 beta-hydroxysteroid dehydrogenaseA K Agarwal, F M Rogerson, T Mune, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1988
Molecular cloning of an inducible serine esterase gene from human cytotoxic lymphocytesJ A Trapani, J L Klein, P C White, et al.Biochemical and Biophysical Research Communications|September 2, 1999
Functional analysis of four CYP21 mutations from spanish patients with congenital adrenal hyperplasiaB S Nunez, M N Lobato, P C White, et al.The Journal of Steroid Biochemistry and Molecular Biology|December 1, 1995
Analysis of the human gene encoding the kidney isozyme of 11 beta-hydroxysteroid dehydrogenaseA K Agarwal, F M Rogerson, T Mune, et al.DNA (Mary Ann Liebert, Inc.)|December 1, 1988
lambda PMV: a bacteriophage vector allowing single-step retrieval of cDNAs following expression in mammalian cellsJ P DiSanto, T N Small, N Flomenberg, et al.Pageof 29