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

J T Epplen

Showing results (81-90 of 365) with videos related to

Pageof 37
Sort By:
Neuroendocrinology|January 1, 1982
Patterns of cyclic AMP phosphodiesterases in the rat pineal gland: sex differences in diurnal rhythmicityJ T Epplen, H Kaltenhäuser, W Engel, et al.
Archiv Fur Kriminologie|July 1, 1990
[Oligonucleotide fingerprinting using (GTG)5 and (GACA)4 probes for the differentiation of body fragments]H Pöche, G Wrobel, V Schneider, et al.
Human Genetics|June 1, 1986
Human DNA sequences isolated with an immunoglobulin switch region probe: sequence, chromosomal localization, and restriction fragment length polymorphismsH Stockinger, J Schmidtke, C Bostock, et al.
Deutsche Medizinische Wochenschrift (1946)|February 24, 1998
[A new rapid test (FISH) for the prenatal diagnosis of the most frequent chromosome aberrations--what significance has it in practice?]B Eiben, W Hammans, R Goebel, et al.
Cytogenetics and Cell Genetics|December 22, 2000
Generalized progressive retinal atrophy of Sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B geneG Dekomien, M Runte, R Gödde, et al.
Immunogenetics|January 1, 1993
Novel members and germline polymorphisms in the human T-cell receptor Vb6 familyM Gomolka, C Epplen, J Buitkamp, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 1, 1995
DNA diagnosis of human genetic individualityS D Pena, V F Prado, J T Epplen
Human Genetics|May 1, 1997
Polymorphisms in the PMP-22 gene region (17p11.2-12) are crucial for simplified diagnosis of duplications/deletionsA Haupt, L Schöls, H Przuntek, et al.
Human Genetics|December 1, 1993
Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25O Riess, C Epplen, I Siedlaczck, et al.
Human Mutation|December 29, 1999
Novel mutation in the RYR1 gene (R2454C) in a patient with malignant hyperthermiaM Gencik, A Gencik, W Mortier, et al.
Pageof 37

Showing results (81-90 of 365) with videos related to

Sort By:
Pageof 37
Neuroendocrinology|January 1, 1982
Patterns of cyclic AMP phosphodiesterases in the rat pineal gland: sex differences in diurnal rhythmicityJ T Epplen, H Kaltenhäuser, W Engel, et al.
Archiv Fur Kriminologie|July 1, 1990
[Oligonucleotide fingerprinting using (GTG)5 and (GACA)4 probes for the differentiation of body fragments]H Pöche, G Wrobel, V Schneider, et al.
Human Genetics|June 1, 1986
Human DNA sequences isolated with an immunoglobulin switch region probe: sequence, chromosomal localization, and restriction fragment length polymorphismsH Stockinger, J Schmidtke, C Bostock, et al.
Deutsche Medizinische Wochenschrift (1946)|February 24, 1998
[A new rapid test (FISH) for the prenatal diagnosis of the most frequent chromosome aberrations--what significance has it in practice?]B Eiben, W Hammans, R Goebel, et al.
Cytogenetics and Cell Genetics|December 22, 2000
Generalized progressive retinal atrophy of Sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B geneG Dekomien, M Runte, R Gödde, et al.
Immunogenetics|January 1, 1993
Novel members and germline polymorphisms in the human T-cell receptor Vb6 familyM Gomolka, C Epplen, J Buitkamp, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 1, 1995
DNA diagnosis of human genetic individualityS D Pena, V F Prado, J T Epplen
Human Genetics|May 1, 1997
Polymorphisms in the PMP-22 gene region (17p11.2-12) are crucial for simplified diagnosis of duplications/deletionsA Haupt, L Schöls, H Przuntek, et al.
Human Genetics|December 1, 1993
Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25O Riess, C Epplen, I Siedlaczck, et al.
Human Mutation|December 29, 1999
Novel mutation in the RYR1 gene (R2454C) in a patient with malignant hyperthermiaM Gencik, A Gencik, W Mortier, et al.
Pageof 37