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

R P Ketterling

Showing results (1-10 of 56) with videos related to

Pageof 6
Sort By:
Human Molecular Genetics|January 1, 1996
The factor IX gene as a model for analysis of human germline mutations: an updateS S Sommer, R P Ketterling
Mutation Research|June 1, 1994
How precisely can data from transgenic mouse mutation-detection systems be extrapolated to humans?: lesions from the human factor IX geneS S Sommer, R P Ketterling
Human Genetics|November 1, 1996
Absence of somatic mosaicism in 17 families with hemophilia B: an analysis with a sensitivity 10- to 1000-fold greater than that of sequencing gelsA Knöll, R P Ketterling, S S Sommer
American Journal of Human Genetics|May 1, 1994
The rates of G:C-->T:A and G:C-->C:G transversions at CpG dinucleotides in the human factor IX geneR P Ketterling, E Vielhaber, S S Sommer
Genomics|August 1, 1991
Evidence that descendants of three founders constitute about 25% of hemophilia B in the United StatesR P Ketterling, C D Bottema, J A Phillips, et al.
Human Mutation|January 1, 1993
Deletions with inversions: report of a mutation and review of the literatureR P Ketterling, D O Ricke, M W Wurster, et al.
Leukemia|October 29, 2004
Development of a D-FISH method to detect DEK/CAN fusion resulting from t(6;9)(p23;q34) in patients with acute myelogenous leukemiaB M Shearer, R A Knudson, H C Flynn, et al.
American Journal of Human Genetics|November 1, 1990
The pattern of factor IX germ-line mutation in Asians is similar to that of CaucasiansC D Bottema, R P Ketterling, H S Yoon, et al.
Human Genetics|May 1, 1992
Missense mutations and the magnitude of functional deficit: the example of factor IXS S Sommer, E J Bowie, R P Ketterling, et al.
Human Genetics|July 1, 1991
T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detectionR P Ketterling, C D Bottema, D D Koeberl, et al.
Pageof 6

Showing results (1-10 of 56) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|January 1, 1996
The factor IX gene as a model for analysis of human germline mutations: an updateS S Sommer, R P Ketterling
Mutation Research|June 1, 1994
How precisely can data from transgenic mouse mutation-detection systems be extrapolated to humans?: lesions from the human factor IX geneS S Sommer, R P Ketterling
Human Genetics|November 1, 1996
Absence of somatic mosaicism in 17 families with hemophilia B: an analysis with a sensitivity 10- to 1000-fold greater than that of sequencing gelsA Knöll, R P Ketterling, S S Sommer
American Journal of Human Genetics|May 1, 1994
The rates of G:C-->T:A and G:C-->C:G transversions at CpG dinucleotides in the human factor IX geneR P Ketterling, E Vielhaber, S S Sommer
Genomics|August 1, 1991
Evidence that descendants of three founders constitute about 25% of hemophilia B in the United StatesR P Ketterling, C D Bottema, J A Phillips, et al.
Human Mutation|January 1, 1993
Deletions with inversions: report of a mutation and review of the literatureR P Ketterling, D O Ricke, M W Wurster, et al.
Leukemia|October 29, 2004
Development of a D-FISH method to detect DEK/CAN fusion resulting from t(6;9)(p23;q34) in patients with acute myelogenous leukemiaB M Shearer, R A Knudson, H C Flynn, et al.
American Journal of Human Genetics|November 1, 1990
The pattern of factor IX germ-line mutation in Asians is similar to that of CaucasiansC D Bottema, R P Ketterling, H S Yoon, et al.
Human Genetics|May 1, 1992
Missense mutations and the magnitude of functional deficit: the example of factor IXS S Sommer, E J Bowie, R P Ketterling, et al.
Human Genetics|July 1, 1991
T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detectionR P Ketterling, C D Bottema, D D Koeberl, et al.
Pageof 6