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

G E Herman

Showing results (71-80 of 92) with videos related to

Pageof 10
Sort By:
Human Molecular Genetics|August 15, 2000
The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locusT Carrel, S M Purandare, W Harrison, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 24, 2007
CHILD syndrome: clinical picture and diagnostic proceduresG Kaminska-Winciorek, L Brzezinska-Wcisło, A Jezela-Stanek, et al.
Somatic Cell and Molecular Genetics|July 1, 1989
Expression of human argininosuccinate synthetase in murine hematopoietic cells in vivoG E Herman, B Jaskoski, P A Wood, et al.
Lancet (London, England)|October 3, 1987
Linkage of tuberous sclerosis to ABO blood groupH Northrup, A L Beaudet, W E O'Brien, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28T A Angel, C J Faust, J C Gonzales, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Mouse X chromosomeY Boyd, G E Herman, P Avner, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1995
Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) geneN G Pasteris, B de Gouyon, A B Cadle, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Encyclopedia of the mouse genome III. October 1993. Mouse X chromosomeS D Brown, P Avner, Y Boyd, et al.
Pediatric Neurology|February 1, 1994
D-2-hydroxyglutaric aciduria in neonate with seizures and CNS dysfunctionW J Craigen, C Jakobs, E A Sekul, et al.
Nature Genetics|July 3, 1999
Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.comJ M Derry, E Gormally, G D Means, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|August 15, 2000
The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locusT Carrel, S M Purandare, W Harrison, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 24, 2007
CHILD syndrome: clinical picture and diagnostic proceduresG Kaminska-Winciorek, L Brzezinska-Wcisło, A Jezela-Stanek, et al.
Somatic Cell and Molecular Genetics|July 1, 1989
Expression of human argininosuccinate synthetase in murine hematopoietic cells in vivoG E Herman, B Jaskoski, P A Wood, et al.
Lancet (London, England)|October 3, 1987
Linkage of tuberous sclerosis to ABO blood groupH Northrup, A L Beaudet, W E O'Brien, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28T A Angel, C J Faust, J C Gonzales, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Mouse X chromosomeY Boyd, G E Herman, P Avner, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1995
Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) geneN G Pasteris, B de Gouyon, A B Cadle, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Encyclopedia of the mouse genome III. October 1993. Mouse X chromosomeS D Brown, P Avner, Y Boyd, et al.
Pediatric Neurology|February 1, 1994
D-2-hydroxyglutaric aciduria in neonate with seizures and CNS dysfunctionW J Craigen, C Jakobs, E A Sekul, et al.
Nature Genetics|July 3, 1999
Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.comJ M Derry, E Gormally, G D Means, et al.
Pageof 10