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

E Passarge

Showing results (91-100 of 151) with videos related to

Pageof 16
Sort By:
American Journal of Human Genetics|March 1, 1980
Rate of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by co-cultivation with normal fibroblastsH W Rüdiger, C R Bartram, W Harder, et al.
Casopis Lekaru Ceskych|October 8, 1982
[The fragile chromosome X syndrome]E Seemanová, E Passarge, A Schmidt, et al.
Human Genetics|September 1, 1989
Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastomaV Greger, E Passarge, W Höpping, et al.
Humangenetik|January 1, 1972
Quinacrine mustard fluorescence of a second Y chromosome in a Y-autosomal translocationS Fründ, T Koske-Westphal, S Fuchs-Mecke, et al.
Tissue Antigens|February 1, 1983
HLA-D and -DR antigens on human amniotic fluid cells. I. Lack of expression of HLA-DE Valentine-Thon, G Kreeb, H Grosse-Wilde, et al.
The Journal of Pediatrics|December 1, 1971
Severe developmental failure with coarse facial features, distal limb hypoplasia, thickened palmar creases, bifid uvula, and ureteral stenosis: a previously unidentified familial disorder with lethal outcomeR A Rüdiger, W Schmidt, D A Loose, et al.
American Journal of Human Genetics|December 1, 1992
A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma geneB Brandt, V Greger, D Yandell, et al.
Nature|March 27, 1975
Letter: Cooling velocity and cell recoveryH W Rüdiger, W Wöhler, H Von Böhmer, et al.
American Journal of Medical Genetics|February 15, 2001
Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2)G Zhu, G Gillessen-Kaesbach, J Wirth, et al.
Annals of Human Genetics|January 1, 1978
Partial trisomy 13 presumably due to recombination in an inversion heterozygote and by unequal crossing-overT Koske-Westphal, R E Pruszak-Seel, R Niss, et al.
Pageof 16

Showing results (91-100 of 151) with videos related to

Sort By:
Pageof 16
American Journal of Human Genetics|March 1, 1980
Rate of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by co-cultivation with normal fibroblastsH W Rüdiger, C R Bartram, W Harder, et al.
Casopis Lekaru Ceskych|October 8, 1982
[The fragile chromosome X syndrome]E Seemanová, E Passarge, A Schmidt, et al.
Human Genetics|September 1, 1989
Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastomaV Greger, E Passarge, W Höpping, et al.
Humangenetik|January 1, 1972
Quinacrine mustard fluorescence of a second Y chromosome in a Y-autosomal translocationS Fründ, T Koske-Westphal, S Fuchs-Mecke, et al.
Tissue Antigens|February 1, 1983
HLA-D and -DR antigens on human amniotic fluid cells. I. Lack of expression of HLA-DE Valentine-Thon, G Kreeb, H Grosse-Wilde, et al.
The Journal of Pediatrics|December 1, 1971
Severe developmental failure with coarse facial features, distal limb hypoplasia, thickened palmar creases, bifid uvula, and ureteral stenosis: a previously unidentified familial disorder with lethal outcomeR A Rüdiger, W Schmidt, D A Loose, et al.
American Journal of Human Genetics|December 1, 1992
A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma geneB Brandt, V Greger, D Yandell, et al.
Nature|March 27, 1975
Letter: Cooling velocity and cell recoveryH W Rüdiger, W Wöhler, H Von Böhmer, et al.
American Journal of Medical Genetics|February 15, 2001
Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2)G Zhu, G Gillessen-Kaesbach, J Wirth, et al.
Annals of Human Genetics|January 1, 1978
Partial trisomy 13 presumably due to recombination in an inversion heterozygote and by unequal crossing-overT Koske-Westphal, R E Pruszak-Seel, R Niss, et al.
Pageof 16