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

B Zabel

Showing results (41-50 of 120) with videos related to

Pageof 12
Sort By:
Pediatric Radiology|January 1, 1994
Kniest dysplasia is caused by dominant collagen II (COL2A1) mutations: parental somatic mosaicism manifesting as Stickler phenotype and mild spondyloepiphyseal dysplasiaJ Spranger, H Menger, S Mundlos, et al.
Klinische Padiatrie|May 1, 1992
[Clinical importance of hepatitis B virus DNA detection in serum of children with chronic hepatitis B]S Wirth, U Möllers, E Schaefer, et al.
The Journal of Clinical Investigation|November 1, 1991
Molecular genetics of intestinal glucose transportE M Wright, E Turk, B Zabel, et al.
Humangenetik|January 1, 1974
Supernumerary small ring chromosomeJ J Hoo, C Forster, I Kindermann, et al.
Genomics|December 10, 1999
Isolation, characterization, and mapping of a zinc finger gene, ZFP95, containing both a SCAN box and an alternatively spliced KRAB A domainS D Dreyer, Q Zheng, B Zabel, et al.
Nature|March 28, 1991
Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporterE Turk, B Zabel, S Mundlos, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
A NOVEL MUTATION ASSOCIATED WITH NEPHROLITIHASIS IN ELLIS-VAN CREVELD SYNDROMEA Kiraz, M A Akin, A Arslan, et al.
The International Journal of Developmental Biology|December 1, 1996
Developmental expression of splicing variants of fibroblast growth factor receptor 3 (FGFR3) in mouseC Wuechner, A C Nordqvist, A Winterpacht, et al.
American Journal of Medical Genetics. Part A|November 20, 2004
A disorder resembling pseudoachondroplasia but without COMP mutationJ W Spranger, B Zabel, J Kennedy, et al.
Hepatology (Baltimore, Md.)|March 30, 1999
Mutations in the basic core promotor and the precore region of hepatitis B virus and their selection in children with fulminant and chronic hepatitis BM Friedt, P Gerner, E Lausch, et al.
Pageof 12

Showing results (41-50 of 120) with videos related to

Sort By:
Pageof 12
Pediatric Radiology|January 1, 1994
Kniest dysplasia is caused by dominant collagen II (COL2A1) mutations: parental somatic mosaicism manifesting as Stickler phenotype and mild spondyloepiphyseal dysplasiaJ Spranger, H Menger, S Mundlos, et al.
Klinische Padiatrie|May 1, 1992
[Clinical importance of hepatitis B virus DNA detection in serum of children with chronic hepatitis B]S Wirth, U Möllers, E Schaefer, et al.
The Journal of Clinical Investigation|November 1, 1991
Molecular genetics of intestinal glucose transportE M Wright, E Turk, B Zabel, et al.
Humangenetik|January 1, 1974
Supernumerary small ring chromosomeJ J Hoo, C Forster, I Kindermann, et al.
Genomics|December 10, 1999
Isolation, characterization, and mapping of a zinc finger gene, ZFP95, containing both a SCAN box and an alternatively spliced KRAB A domainS D Dreyer, Q Zheng, B Zabel, et al.
Nature|March 28, 1991
Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporterE Turk, B Zabel, S Mundlos, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
A NOVEL MUTATION ASSOCIATED WITH NEPHROLITIHASIS IN ELLIS-VAN CREVELD SYNDROMEA Kiraz, M A Akin, A Arslan, et al.
The International Journal of Developmental Biology|December 1, 1996
Developmental expression of splicing variants of fibroblast growth factor receptor 3 (FGFR3) in mouseC Wuechner, A C Nordqvist, A Winterpacht, et al.
American Journal of Medical Genetics. Part A|November 20, 2004
A disorder resembling pseudoachondroplasia but without COMP mutationJ W Spranger, B Zabel, J Kennedy, et al.
Hepatology (Baltimore, Md.)|March 30, 1999
Mutations in the basic core promotor and the precore region of hepatitis B virus and their selection in children with fulminant and chronic hepatitis BM Friedt, P Gerner, E Lausch, et al.
Pageof 12