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J Buckingham

Showing results (91-100 of 126) with videos related to

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Evolution; International Journal of Organic Evolution|March 11, 2006
Relative abundance and the species-specific reinforcement of male mating preference in the Chrysochus (Coleoptera: Chrysomelidae) hybrid zoneMerrill A Peterson, Barbara M Honchak, Stefanie E Locke, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 17, 2013
Multiple mutant T alleles cause haploinsufficiency of Brachyury and short tails in Manx catsKati J Buckingham, Margaret J McMillin, Margaret M Brassil, et al.
World Neurosurgery|April 29, 2020
Correlation Between the Oswestry Disability Index and the North American Spine Surgery Patient Satisfaction IndexTimothy J Yee, Kelsey J Fearer, Mark E Oppenlander, et al.
American Journal of Medical Genetics. Part A|September 1, 2017
Encephalopathy caused by novel mutations in the CMP-sialic acid transporter, SLC35A1Bobby G Ng, Carla G Asteggiano, Martin Kircher, et al.
Genetica|March 31, 2011
Cryptic gametic interactions confer both conspecific and heterospecific advantages in the Chrysochus (Coleoptera: Chrysomelidae) hybrid zoneMerrill A Peterson, Erica L Larson, Margaret Brassil, et al.
American Journal of Medical Genetics. Part A|March 11, 2015
Speech and language in a genotyped cohort of individuals with Kabuki syndromeAngela T Morgan, Cristina Mei, Annette Da Costa, et al.
American Journal of Respiratory Cell and Molecular Biology|April 13, 2021
Inflammasome Genetic Variants, Macrophage Function, and Clinical Outcomes in Cystic FibrosisAndrew D Graustein, William R Berrington, Kati J Buckingham, et al.
Human Molecular Genetics|November 13, 2013
A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complexMarie Estelle Losfeld, Bobby G Ng, Martin Kircher, et al.
American Journal of Medical Genetics. Part A|August 3, 2016
SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset featuresPatricia G Wheeler, Bobby G Ng, Laura Sanford, et al.
Genes, Brain, and Behavior|October 19, 2017
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's diseaseE E Blue, C-E Yu, T A Thornton, et al.
Pageof 13

Showing results (91-100 of 126) with videos related to

Sort By:
Pageof 13
Evolution; International Journal of Organic Evolution|March 11, 2006
Relative abundance and the species-specific reinforcement of male mating preference in the Chrysochus (Coleoptera: Chrysomelidae) hybrid zoneMerrill A Peterson, Barbara M Honchak, Stefanie E Locke, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 17, 2013
Multiple mutant T alleles cause haploinsufficiency of Brachyury and short tails in Manx catsKati J Buckingham, Margaret J McMillin, Margaret M Brassil, et al.
World Neurosurgery|April 29, 2020
Correlation Between the Oswestry Disability Index and the North American Spine Surgery Patient Satisfaction IndexTimothy J Yee, Kelsey J Fearer, Mark E Oppenlander, et al.
American Journal of Medical Genetics. Part A|September 1, 2017
Encephalopathy caused by novel mutations in the CMP-sialic acid transporter, SLC35A1Bobby G Ng, Carla G Asteggiano, Martin Kircher, et al.
Genetica|March 31, 2011
Cryptic gametic interactions confer both conspecific and heterospecific advantages in the Chrysochus (Coleoptera: Chrysomelidae) hybrid zoneMerrill A Peterson, Erica L Larson, Margaret Brassil, et al.
American Journal of Medical Genetics. Part A|March 11, 2015
Speech and language in a genotyped cohort of individuals with Kabuki syndromeAngela T Morgan, Cristina Mei, Annette Da Costa, et al.
American Journal of Respiratory Cell and Molecular Biology|April 13, 2021
Inflammasome Genetic Variants, Macrophage Function, and Clinical Outcomes in Cystic FibrosisAndrew D Graustein, William R Berrington, Kati J Buckingham, et al.
Human Molecular Genetics|November 13, 2013
A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complexMarie Estelle Losfeld, Bobby G Ng, Martin Kircher, et al.
American Journal of Medical Genetics. Part A|August 3, 2016
SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset featuresPatricia G Wheeler, Bobby G Ng, Laura Sanford, et al.
Genes, Brain, and Behavior|October 19, 2017
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's diseaseE E Blue, C-E Yu, T A Thornton, et al.
Pageof 13