Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E Stevenson

Showing results (321-330 of 665) with videos related to

Pageof 67
Sort By:
American Journal of Medical Genetics. Part A|July 19, 2020
Schimke XLID syndrome results from a deletion in BCAP31Raymond J Louie, Debra L Collins, Michael J Friez, et al.
The Plant Journal : for Cell and Molecular Biology|December 22, 2006
Red colouration in apple fruit is due to the activity of the MYB transcription factor, MdMYB10Richard V Espley, Roger P Hellens, Jo Putterill, et al.
Journal of Medical Genetics|June 3, 2006
Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 geneH Lubs, F E Abidi, R Echeverri, et al.
American Journal of Medical Genetics. Part A|January 20, 2009
Elements of morphology: standard terminology for the nose and philtrumRaoul C M Hennekam, Valerie Cormier-Daire, Judith G Hall, et al.
Clinical Genetics|October 30, 2023
Clinical findings in individuals with duplication of genes associated with X-linked intellectual disabilityNikhil Sahajpal, Catherine Ziats, Alka Chaubey, et al.
Conservation Physiology|June 14, 2016
Oxidative stress, activity behaviour and body mass in captive parrotsS D Larcombe, C A Tregaskes, J Coffey, et al.
International Journal of Clinical and Experimental Pathology|July 18, 2014
Features of intraventricular tanycytic ependymoma: report of a case and review of literatureShweta Agarwal, Michael E Stevenson, Michael E Sughrue, et al.
Clinical Genetics|October 1, 1996
Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21B Häne, R J Schroer, J F Arena, et al.
American Journal of Medical Genetics|July 9, 1999
Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22B Häne, R E Stevenson, J F Arena, et al.
Journal of Molecular Biology|May 16, 2001
Two crystal structures of the cytoplasmic molybdate-binding protein ModG suggest a novel cooperative binding mechanism and provide insights into ligand-binding specificityL Delarbre, C E Stevenson, D J White, et al.
Pageof 67

Showing results (321-330 of 665) with videos related to

Sort By:
Pageof 67
American Journal of Medical Genetics. Part A|July 19, 2020
Schimke XLID syndrome results from a deletion in BCAP31Raymond J Louie, Debra L Collins, Michael J Friez, et al.
The Plant Journal : for Cell and Molecular Biology|December 22, 2006
Red colouration in apple fruit is due to the activity of the MYB transcription factor, MdMYB10Richard V Espley, Roger P Hellens, Jo Putterill, et al.
Journal of Medical Genetics|June 3, 2006
Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 geneH Lubs, F E Abidi, R Echeverri, et al.
American Journal of Medical Genetics. Part A|January 20, 2009
Elements of morphology: standard terminology for the nose and philtrumRaoul C M Hennekam, Valerie Cormier-Daire, Judith G Hall, et al.
Clinical Genetics|October 30, 2023
Clinical findings in individuals with duplication of genes associated with X-linked intellectual disabilityNikhil Sahajpal, Catherine Ziats, Alka Chaubey, et al.
Conservation Physiology|June 14, 2016
Oxidative stress, activity behaviour and body mass in captive parrotsS D Larcombe, C A Tregaskes, J Coffey, et al.
International Journal of Clinical and Experimental Pathology|July 18, 2014
Features of intraventricular tanycytic ependymoma: report of a case and review of literatureShweta Agarwal, Michael E Stevenson, Michael E Sughrue, et al.
Clinical Genetics|October 1, 1996
Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21B Häne, R J Schroer, J F Arena, et al.
American Journal of Medical Genetics|July 9, 1999
Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22B Häne, R E Stevenson, J F Arena, et al.
Journal of Molecular Biology|May 16, 2001
Two crystal structures of the cytoplasmic molybdate-binding protein ModG suggest a novel cooperative binding mechanism and provide insights into ligand-binding specificityL Delarbre, C E Stevenson, D J White, et al.
Pageof 67