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

B Horsthemke

Showing results (41-50 of 176) with videos related to

Pageof 18
Sort By:
Cancer Genetics and Cytogenetics|January 1, 1989
Mechanism of i(6p) formation in retinoblastoma tumor cellsB Horsthemke, V Greger, R Becher, et al.
Human Genetics|November 1, 1994
An insertion/deletion polymorphism at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13B Dittrich, K Buiting, S Gross, et al.
Human Molecular Genetics|September 1, 1993
An NciI RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13B Dittrich, S Gross, K Buiting, et al.
Genomics|April 1, 1993
Characterization of a DNA sequence family in the Prader-Willi/Angelman syndrome chromosome region in 15q11-q13B Dittrich, H Knoblauch, K Buiting, et al.
PCR Methods and Applications|May 1, 1992
PCR-mediated cloning of HpaII tiny fragments from microdissected human chromosomesB Horsthemke, U Claussen, S Hesse, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|December 1, 1992
A new restriction fragment length polymorphism of the human TNF-B gene detected by AspHI digestS Ferencik, M Lindemann, B Horsthemke, et al.
Human Genetics|May 1, 1997
The tricho-rhino-phalangeal syndromes: frequency and parental origin of 8q deletionsJ Nardmann, L Tranebjaerg, B Horsthemke, et al.
Bulletin De L'Association Des Anatomistes|June 1, 1991
Construction of band-specific DNA-libraries by microdissection of GTG-banded human chromosomes and universal enzymatic DNA amplificationU Claussen, H J Ludecke, G Senger, et al.
American Journal of Medical Genetics|April 10, 1995
Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotypeG Gillessen-Kaesbach, B Albrecht, E Passarge, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|April 1, 1997
[Molecular genetics and diagnosis of retinoblastoma. Significance for ophthalmologic practice]D R Lohmann, B Brandt, E Passarge, et al.
Pageof 18

Showing results (41-50 of 176) with videos related to

Sort By:
Pageof 18
Cancer Genetics and Cytogenetics|January 1, 1989
Mechanism of i(6p) formation in retinoblastoma tumor cellsB Horsthemke, V Greger, R Becher, et al.
Human Genetics|November 1, 1994
An insertion/deletion polymorphism at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13B Dittrich, K Buiting, S Gross, et al.
Human Molecular Genetics|September 1, 1993
An NciI RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13B Dittrich, S Gross, K Buiting, et al.
Genomics|April 1, 1993
Characterization of a DNA sequence family in the Prader-Willi/Angelman syndrome chromosome region in 15q11-q13B Dittrich, H Knoblauch, K Buiting, et al.
PCR Methods and Applications|May 1, 1992
PCR-mediated cloning of HpaII tiny fragments from microdissected human chromosomesB Horsthemke, U Claussen, S Hesse, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|December 1, 1992
A new restriction fragment length polymorphism of the human TNF-B gene detected by AspHI digestS Ferencik, M Lindemann, B Horsthemke, et al.
Human Genetics|May 1, 1997
The tricho-rhino-phalangeal syndromes: frequency and parental origin of 8q deletionsJ Nardmann, L Tranebjaerg, B Horsthemke, et al.
Bulletin De L'Association Des Anatomistes|June 1, 1991
Construction of band-specific DNA-libraries by microdissection of GTG-banded human chromosomes and universal enzymatic DNA amplificationU Claussen, H J Ludecke, G Senger, et al.
American Journal of Medical Genetics|April 10, 1995
Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotypeG Gillessen-Kaesbach, B Albrecht, E Passarge, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|April 1, 1997
[Molecular genetics and diagnosis of retinoblastoma. Significance for ophthalmologic practice]D R Lohmann, B Brandt, E Passarge, et al.
Pageof 18