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R D Nicholls

Showing results (31-40 of 107) with videos related to

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Nucleic Acids Research|November 11, 1985
Direct cloning of specific genomic DNA sequences in plasmid libraries following fragment enrichmentR D Nicholls, A V Hill, J B Clegg, et al.
Molecular Human Reproduction|April 1, 1997
Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromesC C Glenn, D J Driscoll, T P Yang, et al.
The EMBO Journal|April 1, 1987
Non-methylated CpG-rich islands at the human alpha-globin locus: implications for evolution of the alpha-globin pseudogeneA P Bird, M H Taggart, R D Nicholls, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromesK Buiting, S Gross, Y Ji, et al.
American Journal of Human Genetics|January 1, 1991
Chromosome 15 uniparental disomy is not frequent in Angelman syndromeJ H Knoll, K A Glatt, R D Nicholls, et al.
Nature|November 16, 1989
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndromeR D Nicholls, J H Knoll, M G Butler, et al.
Human Molecular Genetics|October 1, 1994
A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical regionJ Gabriel, W Gottlieb, A Garcia, et al.
British Journal of Haematology|August 1, 1987
Characterization of a new alpha zero thalassaemia defect in the South African populationS Vandenplas, D R Higgs, R D Nicholls, et al.
Genomics|March 20, 1995
Organization and sequence of the human P gene and identification of a new family of transport proteinsS T Lee, R D Nicholls, M T Jong, et al.
American Journal of Medical Genetics|January 11, 1996
DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi regionP A Mowery-Rushton, D J Driscoll, R D Nicholls, et al.
Pageof 11

Showing results (31-40 of 107) with videos related to

Sort By:
Pageof 11
Nucleic Acids Research|November 11, 1985
Direct cloning of specific genomic DNA sequences in plasmid libraries following fragment enrichmentR D Nicholls, A V Hill, J B Clegg, et al.
Molecular Human Reproduction|April 1, 1997
Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromesC C Glenn, D J Driscoll, T P Yang, et al.
The EMBO Journal|April 1, 1987
Non-methylated CpG-rich islands at the human alpha-globin locus: implications for evolution of the alpha-globin pseudogeneA P Bird, M H Taggart, R D Nicholls, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromesK Buiting, S Gross, Y Ji, et al.
American Journal of Human Genetics|January 1, 1991
Chromosome 15 uniparental disomy is not frequent in Angelman syndromeJ H Knoll, K A Glatt, R D Nicholls, et al.
Nature|November 16, 1989
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndromeR D Nicholls, J H Knoll, M G Butler, et al.
Human Molecular Genetics|October 1, 1994
A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical regionJ Gabriel, W Gottlieb, A Garcia, et al.
British Journal of Haematology|August 1, 1987
Characterization of a new alpha zero thalassaemia defect in the South African populationS Vandenplas, D R Higgs, R D Nicholls, et al.
Genomics|March 20, 1995
Organization and sequence of the human P gene and identification of a new family of transport proteinsS T Lee, R D Nicholls, M T Jong, et al.
American Journal of Medical Genetics|January 11, 1996
DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi regionP A Mowery-Rushton, D J Driscoll, R D Nicholls, et al.
Pageof 11