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Genomics

Showing results (171-180 of 10,746) with videos related to

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Genomics|October 1, 1989
Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21BP A Donohoue, N Jospe, C J Migeon, et al.
Genomics|October 1, 1989
A multigene deletion in the human IGH constant region locus involves highly homologous hot spots of recombinationG Keyeux, G Lefranc, M P Lefranc
Genomics|October 1, 1989
Gene mapping by enzymatic amplification from flow-sorted chromosomesF Cotter, S Nasipuri, G Lam, et al.
Genomics|October 1, 1989
Chromosomal localization of murine interleukin-1 alpha and beta genesJ Boultwood, G Breckon, D Birch, et al.
Genomics|October 1, 1989
Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplificationW C Nichols, J J Liepnieks, V A McKusick, et al.
Genomics|October 1, 1989
Chromosomal localization of DBL oncogene sequencesS R Tronick, O W McBride, N C Popescu, et al.
Genomics|October 1, 1989
Localization of three DNA segments encompassing tRNA genes to human chromosomes 1, 5, and 16: proposed mechanism and significance of tRNA gene dispersionO W McBride, I L Pirtle, R M Pirtle
Genomics|October 1, 1989
Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophiesH Gilgenkrantz, J Chelly, M Lambert, et al.
Genomics|October 1, 1989
Chromosomal mapping and nucleotide sequence of a human DNA autonomously replicating sequenceM Aguinaga, C Sharan, D N Singh, et al.
Genomics|October 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21G J Farrar, P McWilliam, E M Sharp, et al.
Pageof 1,075

Showing results (171-180 of 10,746) with videos related to

Sort By:
Pageof 1,075
Genomics|October 1, 1989
Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21BP A Donohoue, N Jospe, C J Migeon, et al.
Genomics|October 1, 1989
A multigene deletion in the human IGH constant region locus involves highly homologous hot spots of recombinationG Keyeux, G Lefranc, M P Lefranc
Genomics|October 1, 1989
Gene mapping by enzymatic amplification from flow-sorted chromosomesF Cotter, S Nasipuri, G Lam, et al.
Genomics|October 1, 1989
Chromosomal localization of murine interleukin-1 alpha and beta genesJ Boultwood, G Breckon, D Birch, et al.
Genomics|October 1, 1989
Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplificationW C Nichols, J J Liepnieks, V A McKusick, et al.
Genomics|October 1, 1989
Chromosomal localization of DBL oncogene sequencesS R Tronick, O W McBride, N C Popescu, et al.
Genomics|October 1, 1989
Localization of three DNA segments encompassing tRNA genes to human chromosomes 1, 5, and 16: proposed mechanism and significance of tRNA gene dispersionO W McBride, I L Pirtle, R M Pirtle
Genomics|October 1, 1989
Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophiesH Gilgenkrantz, J Chelly, M Lambert, et al.
Genomics|October 1, 1989
Chromosomal mapping and nucleotide sequence of a human DNA autonomously replicating sequenceM Aguinaga, C Sharan, D N Singh, et al.
Genomics|October 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21G J Farrar, P McWilliam, E M Sharp, et al.
Pageof 1,075