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

M Stumm

Showing results (21-30 of 57) with videos related to

Pageof 6
Sort By:
Oncology Research|April 10, 2002
Molecular characterization of the DICE1 (DDX26) tumor suppressor gene in lung carcinoma cellsI Wieland, A Röpke, M Stumm, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Female pseudohermaphroditism caused by caudal dysgenesisP Wieacker, U Grumpelt, T Schulz, et al.
Journal of Medical Genetics|February 12, 2002
Partial trisomy 9p12p21.3 with a normal phenotypeM Stumm, J Müsebeck, H Tönnies, et al.
Hepatology (Baltimore, Md.)|March 30, 1999
Increased angiogenesis in portal hypertensive rats: role of nitric oxideL T Sumanovski, E Battegay, M Stumm, et al.
American Journal of Clinical Pathology|February 17, 2012
Validation of a postfixation tissue storage and transport medium to preserve histopathology and molecular pathology analyses (total and phosphoactivated proteins, and FISH)Michael M Stumm, Maja R Walker, Caroline Stork, et al.
Bioorganicheskaia Khimiia|March 14, 1998
[Structure and chromosomal localization of human neurogranin gene]I B Mertsalov, M Stumm, P Wieacker, et al.
Cancer Genetics and Cytogenetics|May 10, 2001
No evidence for deletions of the NBS1 gene in lymphomasM Stumm, A von Ruskowsky, R Siebert, et al.
Fetal Diagnosis and Therapy|February 18, 2010
First-trimester prenatal diagnosis of Okihiro syndromeR Becker, D Horn, U Knoll, et al.
American Journal of Medical Genetics|December 18, 1998
Familial occurrence of a del(Xp-) chromosome: pitfall in karyotype/phenotype correlationA Soyke, M Stumm, P Krebs, et al.
Journal of Medical Genetics|June 5, 2001
Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISHH Tönnies, M Stumm, L Neumann, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Oncology Research|April 10, 2002
Molecular characterization of the DICE1 (DDX26) tumor suppressor gene in lung carcinoma cellsI Wieland, A Röpke, M Stumm, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Female pseudohermaphroditism caused by caudal dysgenesisP Wieacker, U Grumpelt, T Schulz, et al.
Journal of Medical Genetics|February 12, 2002
Partial trisomy 9p12p21.3 with a normal phenotypeM Stumm, J Müsebeck, H Tönnies, et al.
Hepatology (Baltimore, Md.)|March 30, 1999
Increased angiogenesis in portal hypertensive rats: role of nitric oxideL T Sumanovski, E Battegay, M Stumm, et al.
American Journal of Clinical Pathology|February 17, 2012
Validation of a postfixation tissue storage and transport medium to preserve histopathology and molecular pathology analyses (total and phosphoactivated proteins, and FISH)Michael M Stumm, Maja R Walker, Caroline Stork, et al.
Bioorganicheskaia Khimiia|March 14, 1998
[Structure and chromosomal localization of human neurogranin gene]I B Mertsalov, M Stumm, P Wieacker, et al.
Cancer Genetics and Cytogenetics|May 10, 2001
No evidence for deletions of the NBS1 gene in lymphomasM Stumm, A von Ruskowsky, R Siebert, et al.
Fetal Diagnosis and Therapy|February 18, 2010
First-trimester prenatal diagnosis of Okihiro syndromeR Becker, D Horn, U Knoll, et al.
American Journal of Medical Genetics|December 18, 1998
Familial occurrence of a del(Xp-) chromosome: pitfall in karyotype/phenotype correlationA Soyke, M Stumm, P Krebs, et al.
Journal of Medical Genetics|June 5, 2001
Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISHH Tönnies, M Stumm, L Neumann, et al.
Pageof 6