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

K Grade

Showing results (21-30 of 33) with videos related to

Pageof 4
Sort By:
Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 11, 2005
Role of Drosophila HP1 in euchromatic gene expressionDiane E Cryderman, Stephanie K Grade, Yuhong Li, et al.
Nucleic Acids Research|September 12, 1989
Polymerase chain reaction for detection of the pMP6d-9/MspI RFLP, a marker closely linked to the cystic fibrosis mutationA Huth, X Estivill, K Grade, et al.
Acta Universitatis Carolinae. Medica|January 1, 1990
Prenatal diagnosis of cystic fibrosis in first and second trimenon (GDR report)R Szibor, R Brückner, J Gedschold, et al.
Pathologie-Biologie|June 1, 1991
CF DNA-diagnosis and gene mutation analysis: data from East GermanyC Coutelle, K Grade, R Brückner, et al.
Human Mutation|January 1, 1992
Prevalence of cystic fibrosis mutations in the East German populationC Coutelle, R Brückner, K Grade, et al.
Acta Universitatis Carolinae. Medica|January 1, 1990
Distribution of RFLP haplotypes in CF in relation to clinical courseJ Gedschold, R Brückner, R Szibor, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
Present state of DNA-diagnosis for cystic fibrosis and attitudes concerning a heterozygote screening in the GDRC Coutelle, K Grade, A Speer, et al.
Human Genetics|September 1, 1990
First analysis of the F508 deletion in cystic fibrosis patients from the GDRK Grade, K Will, R Szibor, et al.
Journal of Medical Genetics|November 1, 1990
Deletion analysis of DMD/BMD families from the German Democratic Republic and selected regions of Czechoslovakia and HungaryA Speer, U Kräft, R Hanke, et al.
Journal of Medical Genetics|January 1, 1989
Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probesA Speer, A W Spiegler, R Hanke, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 11, 2005
Role of Drosophila HP1 in euchromatic gene expressionDiane E Cryderman, Stephanie K Grade, Yuhong Li, et al.
Nucleic Acids Research|September 12, 1989
Polymerase chain reaction for detection of the pMP6d-9/MspI RFLP, a marker closely linked to the cystic fibrosis mutationA Huth, X Estivill, K Grade, et al.
Acta Universitatis Carolinae. Medica|January 1, 1990
Prenatal diagnosis of cystic fibrosis in first and second trimenon (GDR report)R Szibor, R Brückner, J Gedschold, et al.
Pathologie-Biologie|June 1, 1991
CF DNA-diagnosis and gene mutation analysis: data from East GermanyC Coutelle, K Grade, R Brückner, et al.
Human Mutation|January 1, 1992
Prevalence of cystic fibrosis mutations in the East German populationC Coutelle, R Brückner, K Grade, et al.
Acta Universitatis Carolinae. Medica|January 1, 1990
Distribution of RFLP haplotypes in CF in relation to clinical courseJ Gedschold, R Brückner, R Szibor, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
Present state of DNA-diagnosis for cystic fibrosis and attitudes concerning a heterozygote screening in the GDRC Coutelle, K Grade, A Speer, et al.
Human Genetics|September 1, 1990
First analysis of the F508 deletion in cystic fibrosis patients from the GDRK Grade, K Will, R Szibor, et al.
Journal of Medical Genetics|November 1, 1990
Deletion analysis of DMD/BMD families from the German Democratic Republic and selected regions of Czechoslovakia and HungaryA Speer, U Kräft, R Hanke, et al.
Journal of Medical Genetics|January 1, 1989
Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probesA Speer, A W Spiegler, R Hanke, et al.
Pageof 4