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

N Tommerup

Showing results (61-70 of 179) with videos related to

Pageof 18
Sort By:
Cytogenetics and Cell Genetics|August 31, 2000
Assignment of the NR2E3 gene to mouse chromosome 9 and to human chromosome 15q22.33-->q23N D Rendtorff, H Vissing, Z Tümer, et al.
Journal of Medical Genetics|October 1, 1986
Segregation of a t(3;20) translocation through three generations resulting in unbalanced karyotypes in six personsK B Nielsen, N Tommerup, B Jespersen, et al.
Cancer Genetics and Cytogenetics|August 5, 1998
Occurrence of cancer in a cohort of 183 persons with constitutional chromosome 7 abnormalitiesH Hasle, J H Olsen, J Hansen, et al.
Cancer Genetics and Cytogenetics|August 1, 1987
DNA-aneuploidy in 46,XX hydatidiform molesL O Vejerslev, J K Larsen, I J Christensen, et al.
American Journal of Medical Genetics|April 1, 1988
Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patientsL Tranebjaerg, K B Nielsen, N Tommerup, et al.
Immunogenetics|September 1, 1999
Structural organization, tissue expression, and chromosomal localization of Ciao 1, a functional modulator of the Wilms' tumor suppressor, WT1R W Johnstone, N Tommerup, C Hansen, et al.
Clinical Genetics|August 27, 2014
The first mutation in CNGA2 in two brothers with anosmiaH G Karstensen, Y Mang, T Fark, et al.
Clinical Genetics|September 1, 1983
Folic acid metabolism in a patient with fragile XK Brøndum Nielsen, N Tommerup, B Friis, et al.
Journal of Medical Genetics|February 1, 1987
New assignment of the adenosine deaminase gene locus to chromosome 20q13 X 11 by study of a patient with interstitial deletion 20qM B Petersen, L Tranebjaerg, N Tommerup, et al.
Ugeskrift for Laeger|July 6, 1981
[Mental retardation, macroorchidism and hereditary X-chromosome abnormality, fra(X) (q28). A new syndrome]K B Nielsen, J Lindholt, N Tommerup, et al.
Pageof 18

Showing results (61-70 of 179) with videos related to

Sort By:
Pageof 18
Cytogenetics and Cell Genetics|August 31, 2000
Assignment of the NR2E3 gene to mouse chromosome 9 and to human chromosome 15q22.33-->q23N D Rendtorff, H Vissing, Z Tümer, et al.
Journal of Medical Genetics|October 1, 1986
Segregation of a t(3;20) translocation through three generations resulting in unbalanced karyotypes in six personsK B Nielsen, N Tommerup, B Jespersen, et al.
Cancer Genetics and Cytogenetics|August 5, 1998
Occurrence of cancer in a cohort of 183 persons with constitutional chromosome 7 abnormalitiesH Hasle, J H Olsen, J Hansen, et al.
Cancer Genetics and Cytogenetics|August 1, 1987
DNA-aneuploidy in 46,XX hydatidiform molesL O Vejerslev, J K Larsen, I J Christensen, et al.
American Journal of Medical Genetics|April 1, 1988
Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patientsL Tranebjaerg, K B Nielsen, N Tommerup, et al.
Immunogenetics|September 1, 1999
Structural organization, tissue expression, and chromosomal localization of Ciao 1, a functional modulator of the Wilms' tumor suppressor, WT1R W Johnstone, N Tommerup, C Hansen, et al.
Clinical Genetics|August 27, 2014
The first mutation in CNGA2 in two brothers with anosmiaH G Karstensen, Y Mang, T Fark, et al.
Clinical Genetics|September 1, 1983
Folic acid metabolism in a patient with fragile XK Brøndum Nielsen, N Tommerup, B Friis, et al.
Journal of Medical Genetics|February 1, 1987
New assignment of the adenosine deaminase gene locus to chromosome 20q13 X 11 by study of a patient with interstitial deletion 20qM B Petersen, L Tranebjaerg, N Tommerup, et al.
Ugeskrift for Laeger|July 6, 1981
[Mental retardation, macroorchidism and hereditary X-chromosome abnormality, fra(X) (q28). A new syndrome]K B Nielsen, J Lindholt, N Tommerup, et al.
Pageof 18