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H F Willard

Showing results (41-50 of 248) with videos related to

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Science (New York, N.Y.)|November 22, 1985
Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disordersH F Willard, J R Riordan
American Journal of Human Genetics|September 1, 1987
Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosomeS J Durfy, H F Willard
Nucleic Acids Research|April 25, 1985
Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosomeJ S Waye, H F Willard
Biochemical and Biophysical Research Communications|October 10, 1977
Inherited deficiencies of human methylmalonyl CaA mutase activity: reduced affinity of mutant apoenzyme for adenosylcobalaminH F Willard, L E Rosenberg
Journal of Molecular Evolution|December 1, 1995
Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: evidence for concerted evolution along haplotypic lineagesP E Warburton, H F Willard
Human Molecular Genetics|April 1, 1993
A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat lociM M Mahtani, H F Willard
Human Genetics|October 1, 1990
The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysisV M Watt, H F Willard
American Journal of Human Genetics|May 1, 1976
Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopyH F Willard, S A Latt
The Journal of Cell Biology|March 27, 2001
A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosomeB P Chadwick, H F Willard
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 26, 2000
Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and humanK D Tsuchiya, H F Willard
Pageof 25

Showing results (41-50 of 248) with videos related to

Sort By:
Pageof 25
Science (New York, N.Y.)|November 22, 1985
Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disordersH F Willard, J R Riordan
American Journal of Human Genetics|September 1, 1987
Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosomeS J Durfy, H F Willard
Nucleic Acids Research|April 25, 1985
Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosomeJ S Waye, H F Willard
Biochemical and Biophysical Research Communications|October 10, 1977
Inherited deficiencies of human methylmalonyl CaA mutase activity: reduced affinity of mutant apoenzyme for adenosylcobalaminH F Willard, L E Rosenberg
Journal of Molecular Evolution|December 1, 1995
Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: evidence for concerted evolution along haplotypic lineagesP E Warburton, H F Willard
Human Molecular Genetics|April 1, 1993
A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat lociM M Mahtani, H F Willard
Human Genetics|October 1, 1990
The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysisV M Watt, H F Willard
American Journal of Human Genetics|May 1, 1976
Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopyH F Willard, S A Latt
The Journal of Cell Biology|March 27, 2001
A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosomeB P Chadwick, H F Willard
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 26, 2000
Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and humanK D Tsuchiya, H F Willard
Pageof 25