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

A Haas

Showing results (691-700 of 1,838) with videos related to

Pageof 184
Sort By:
Annales De Genetique|May 4, 2001
Microdissection and reverse painting reveals a microdeletion 6(q26qter) in a de novo r(6) chromosomeR Birnbacher, I Chudoba, H Pirc-Danoewinata, et al.
Cancer Genetics and Cytogenetics|June 1, 1996
MLL/ENL fusion in congenital acute lymphoblastic leukemia with a unique t(11;18;19)M Horstmann, A Argyriou-Tirita, A Borkhardt, et al.
Pediatric Blood & Cancer|September 27, 2021
Clinical outcomes for pediatric patients receiving radiotherapy for solid tumor central nervous system metastasesThomas P Howard, Patrick J Boyle, Karen J Marcus, et al.
Cancer Research|September 10, 1998
Ionizing radiation inhibits chemotherapy-induced apoptosis in cultured glioma cells: implications for combined modality therapyG L Yount, D A Haas-Kogan, K S Levine, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 3, 2007
Primary pigmented nodular adrenocortical disease (PPNAD) and pituitary adenoma in a boy with sporadic Carney complex due to a novel, de novo paternal PRKAR1A mutation (R96X)Christian Urban, Andreas Weinhäusel, Peter Fritsch, et al.
European Neurology|January 1, 1992
Parlodel SRO in Parkinson's disease: a double-blind randomized comparison of Parlodel standard and Parlodel SROE N Jansen, A Staal-Schreinemachers, J J van der Sande, et al.
Virchows Archiv : an International Journal of Pathology|March 12, 2005
Evidence of a polyclonal nature of myositis ossificansAndreas Leithner, Andreas Weinhaeusel, Petra Zeitlhofer, et al.
Genes, Chromosomes & Cancer|September 1, 1994
Detection of numerical and structural chromosome abnormalities in pediatric germ cell tumors by means of interphase cytogeneticsC Stock, I M Ambros, T Lion, et al.
Radiation Research|March 1, 1996
Cytogenetic damage and the radiation-induced G1-phase checkpointN Gupta, R Vij, D A Haas-Kogan, et al.
Pediatric Research|March 17, 2009
Myocardial inflammation, cellular death, and viral detection in sudden infant death caused by SIDS, suffocation, or myocarditisHenry F Krous, Christine Ferandos, Homeyra Masoumi, et al.
Pageof 184

Showing results (691-700 of 1,838) with videos related to

Sort By:
Pageof 184
Annales De Genetique|May 4, 2001
Microdissection and reverse painting reveals a microdeletion 6(q26qter) in a de novo r(6) chromosomeR Birnbacher, I Chudoba, H Pirc-Danoewinata, et al.
Cancer Genetics and Cytogenetics|June 1, 1996
MLL/ENL fusion in congenital acute lymphoblastic leukemia with a unique t(11;18;19)M Horstmann, A Argyriou-Tirita, A Borkhardt, et al.
Pediatric Blood & Cancer|September 27, 2021
Clinical outcomes for pediatric patients receiving radiotherapy for solid tumor central nervous system metastasesThomas P Howard, Patrick J Boyle, Karen J Marcus, et al.
Cancer Research|September 10, 1998
Ionizing radiation inhibits chemotherapy-induced apoptosis in cultured glioma cells: implications for combined modality therapyG L Yount, D A Haas-Kogan, K S Levine, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 3, 2007
Primary pigmented nodular adrenocortical disease (PPNAD) and pituitary adenoma in a boy with sporadic Carney complex due to a novel, de novo paternal PRKAR1A mutation (R96X)Christian Urban, Andreas Weinhäusel, Peter Fritsch, et al.
European Neurology|January 1, 1992
Parlodel SRO in Parkinson's disease: a double-blind randomized comparison of Parlodel standard and Parlodel SROE N Jansen, A Staal-Schreinemachers, J J van der Sande, et al.
Virchows Archiv : an International Journal of Pathology|March 12, 2005
Evidence of a polyclonal nature of myositis ossificansAndreas Leithner, Andreas Weinhaeusel, Petra Zeitlhofer, et al.
Genes, Chromosomes & Cancer|September 1, 1994
Detection of numerical and structural chromosome abnormalities in pediatric germ cell tumors by means of interphase cytogeneticsC Stock, I M Ambros, T Lion, et al.
Radiation Research|March 1, 1996
Cytogenetic damage and the radiation-induced G1-phase checkpointN Gupta, R Vij, D A Haas-Kogan, et al.
Pediatric Research|March 17, 2009
Myocardial inflammation, cellular death, and viral detection in sudden infant death caused by SIDS, suffocation, or myocarditisHenry F Krous, Christine Ferandos, Homeyra Masoumi, et al.
Pageof 184