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Michael Bober

Showing results (1-10 of 12) with videos related to

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American Journal of Medical Genetics. Part A|July 31, 2008
Scott sign: a clinical measure of ligamentous laxity in achondroplastic infantsMichael Bober, Caitlyn Johnson, Linda Nicholson, et al.
Seminars in Arthritis and Rheumatism|December 27, 2008
Maternal mixed connective tissue disease and offspring with chondrodysplasia punctataSteffan W Schulz, Michael Bober, Caitlyn Johnson, et al.
Bioinformatics (Oxford, England)|July 16, 2002
CaGE: cardiac gene expression knowledgebaseMichael Bober, Kevin Wiehe, Christina Yung, et al.
American Journal of Medical Genetics. Part A|December 22, 2017
The expanding phenotype of RNU4ATAC pathogenic variants to Lowry Wood syndromeLaura S Farach, Mary E Little, Angela L Duker, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataractsKaren W Gripp, Caitlyn Johnson, Charles I Scott, et al.
Spine|August 8, 2013
Growth-sparing spinal instrumentation in skeletal dysplasiaAli F Karatas, Ozgur Dede, Kenneth Rogers, et al.
Current Biology : CB|September 16, 2014
A unique set of centrosome proteins requires pericentrin for spindle-pole localization and spindle orientationChun-Ting Chen, Heidi Hehnly, Qing Yu, et al.
Nature Genetics|March 2, 2011
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndromeLouise S Bicknell, Sarah Walker, Anna Klingseisen, et al.
American Journal of Medical Genetics. Part A|March 19, 2008
Clinical and molecular analysis of arylsulfatase E in patients with brachytelephalangic chondrodysplasia punctataMichelle Nino, Claudia Matos-Miranda, Momoe Maeda, et al.
Diabetes|January 29, 2011
Genetic defects in human pericentrin are associated with severe insulin resistance and diabetesIsabel Huang-Doran, Louise S Bicknell, Francis M Finucane, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|July 31, 2008
Scott sign: a clinical measure of ligamentous laxity in achondroplastic infantsMichael Bober, Caitlyn Johnson, Linda Nicholson, et al.
Seminars in Arthritis and Rheumatism|December 27, 2008
Maternal mixed connective tissue disease and offspring with chondrodysplasia punctataSteffan W Schulz, Michael Bober, Caitlyn Johnson, et al.
Bioinformatics (Oxford, England)|July 16, 2002
CaGE: cardiac gene expression knowledgebaseMichael Bober, Kevin Wiehe, Christina Yung, et al.
American Journal of Medical Genetics. Part A|December 22, 2017
The expanding phenotype of RNU4ATAC pathogenic variants to Lowry Wood syndromeLaura S Farach, Mary E Little, Angela L Duker, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataractsKaren W Gripp, Caitlyn Johnson, Charles I Scott, et al.
Spine|August 8, 2013
Growth-sparing spinal instrumentation in skeletal dysplasiaAli F Karatas, Ozgur Dede, Kenneth Rogers, et al.
Current Biology : CB|September 16, 2014
A unique set of centrosome proteins requires pericentrin for spindle-pole localization and spindle orientationChun-Ting Chen, Heidi Hehnly, Qing Yu, et al.
Nature Genetics|March 2, 2011
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndromeLouise S Bicknell, Sarah Walker, Anna Klingseisen, et al.
American Journal of Medical Genetics. Part A|March 19, 2008
Clinical and molecular analysis of arylsulfatase E in patients with brachytelephalangic chondrodysplasia punctataMichelle Nino, Claudia Matos-Miranda, Momoe Maeda, et al.
Diabetes|January 29, 2011
Genetic defects in human pericentrin are associated with severe insulin resistance and diabetesIsabel Huang-Doran, Louise S Bicknell, Francis M Finucane, et al.
Pageof 2