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H F Willard

Showing results (31-40 of 248) with videos related to

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Genomics|August 1, 1993
Pulsed-field map of Xq13 in the region of the human X inactivation centerR G Lafrenière, H F Willard
Current Opinion in Genetics & Development|June 1, 1993
Mammalian chromosome structureC Tyler-Smith, H F Willard
Somatic Cell Genetics|March 1, 1980
Human X chromosomes: synchrony of DNA replication in diploid and triploid fibroblasts with multiple active or inactive X chromosomesH F Willard, W R Breg
The Journal of Clinical Investigation|March 1, 1980
Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expressionH F Willard, L E Rosenberg
Archives of Biochemistry and Biophysics|March 1, 1980
Interactions of methylmalonyl CoA mutase from normal human fibroblasts with adenosylcobalamin and methylmalonyl CoA: evidence for non-equivalent active sitesH F Willard, L E Rosenberg
American Journal of Human Genetics|February 1, 1990
Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivationC J Brown, H F Willard
Nature Genetics|November 7, 1998
Stable dicentric X chromosomes with two functional centromeresB A Sullivan, H F Willard
Nucleic Acids Research|September 25, 1987
Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomesJ S Waye, H F Willard
Journal of Molecular Biology|December 5, 1990
Concerted evolution of primate alpha satellite DNA. Evidence for an ancestral sequence shared by gorilla and human X chromosome alpha satelliteS J Durfy, H F Willard
Nucleic Acids Research|September 11, 1986
Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixationJ S Waye, H F Willard
Pageof 25

Showing results (31-40 of 248) with videos related to

Sort By:
Pageof 25
Genomics|August 1, 1993
Pulsed-field map of Xq13 in the region of the human X inactivation centerR G Lafrenière, H F Willard
Current Opinion in Genetics & Development|June 1, 1993
Mammalian chromosome structureC Tyler-Smith, H F Willard
Somatic Cell Genetics|March 1, 1980
Human X chromosomes: synchrony of DNA replication in diploid and triploid fibroblasts with multiple active or inactive X chromosomesH F Willard, W R Breg
The Journal of Clinical Investigation|March 1, 1980
Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expressionH F Willard, L E Rosenberg
Archives of Biochemistry and Biophysics|March 1, 1980
Interactions of methylmalonyl CoA mutase from normal human fibroblasts with adenosylcobalamin and methylmalonyl CoA: evidence for non-equivalent active sitesH F Willard, L E Rosenberg
American Journal of Human Genetics|February 1, 1990
Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivationC J Brown, H F Willard
Nature Genetics|November 7, 1998
Stable dicentric X chromosomes with two functional centromeresB A Sullivan, H F Willard
Nucleic Acids Research|September 25, 1987
Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomesJ S Waye, H F Willard
Journal of Molecular Biology|December 5, 1990
Concerted evolution of primate alpha satellite DNA. Evidence for an ancestral sequence shared by gorilla and human X chromosome alpha satelliteS J Durfy, H F Willard
Nucleic Acids Research|September 11, 1986
Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixationJ S Waye, H F Willard
Pageof 25