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 Olek

Showing results (31-40 of 115) with videos related to

Pageof 12
Sort By:
Genetika|August 1, 1995
[A new point mutation in the mitochondrial gene ND1, detected in a patient with type II diabetes]V N Kalinin, W Schmidt, W Poller, et al.
Human Genetics|January 1, 1979
Assignment of a gene for human quinoid-dihydropteridine reductase (QDPR, EC 1.6.5.1) to chromosome 4P Kuhl, K Olek, P Wardenbach, et al.
Human Genetics|March 1, 1991
DNA polymorphisms associated with a new alpha 1-antitrypsin PIQ0 variant (PIQ0riedenburg)W Poller, J P Faber, S Weidinger, et al.
American Journal of Human Genetics|January 1, 1992
Parental origin of factor IX gene mutations, and their distribution in the geneM Ludwig, T Grimm, H H Brackmann, et al.
Human Genetics|January 1, 1992
Cloning of the human alpha 2-macroglobulin gene and detection of mutations in two functional domains: the bait region and the thiolester siteW Poller, J P Faber, G Klobeck, et al.
Human Genetics|February 1, 1992
Allelic dimorphism in the human tissue-type plasminogen activator (TPA) gene as a result of an Alu insertion/deletion eventM Ludwig, K D Wohn, W D Schleuning, et al.
The Clinical Investigator|May 1, 1994
Myotonic dystrophy and limb girdle muscular dystrophy in one familyR Schröder, S Beyenburg, J Weber, et al.
European Review for Medical and Pharmacological Sciences|September 22, 2016
Pruritus in selected dermatosesK Olek-Hrab, M Hrab, J Szyfter-Harris, et al.
Neurology|April 23, 2003
Carnitine palmitoyltransferase II deficiency: molecular and biochemical analysis of 32 patientsT Wieser, M Deschauer, K Olek, et al.
Doklady Akademii Nauk|August 1, 1995
[Allele-specific sequencing]V N Kalinin, K Olek, W Schmidt, et al.
Pageof 12

Showing results (31-40 of 115) with videos related to

Sort By:
Pageof 12
Genetika|August 1, 1995
[A new point mutation in the mitochondrial gene ND1, detected in a patient with type II diabetes]V N Kalinin, W Schmidt, W Poller, et al.
Human Genetics|January 1, 1979
Assignment of a gene for human quinoid-dihydropteridine reductase (QDPR, EC 1.6.5.1) to chromosome 4P Kuhl, K Olek, P Wardenbach, et al.
Human Genetics|March 1, 1991
DNA polymorphisms associated with a new alpha 1-antitrypsin PIQ0 variant (PIQ0riedenburg)W Poller, J P Faber, S Weidinger, et al.
American Journal of Human Genetics|January 1, 1992
Parental origin of factor IX gene mutations, and their distribution in the geneM Ludwig, T Grimm, H H Brackmann, et al.
Human Genetics|January 1, 1992
Cloning of the human alpha 2-macroglobulin gene and detection of mutations in two functional domains: the bait region and the thiolester siteW Poller, J P Faber, G Klobeck, et al.
Human Genetics|February 1, 1992
Allelic dimorphism in the human tissue-type plasminogen activator (TPA) gene as a result of an Alu insertion/deletion eventM Ludwig, K D Wohn, W D Schleuning, et al.
The Clinical Investigator|May 1, 1994
Myotonic dystrophy and limb girdle muscular dystrophy in one familyR Schröder, S Beyenburg, J Weber, et al.
European Review for Medical and Pharmacological Sciences|September 22, 2016
Pruritus in selected dermatosesK Olek-Hrab, M Hrab, J Szyfter-Harris, et al.
Neurology|April 23, 2003
Carnitine palmitoyltransferase II deficiency: molecular and biochemical analysis of 32 patientsT Wieser, M Deschauer, K Olek, et al.
Doklady Akademii Nauk|August 1, 1995
[Allele-specific sequencing]V N Kalinin, K Olek, W Schmidt, et al.
Pageof 12