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

T Celkan

Showing results (11-20 of 15) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 15 results.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2NE Berber, I D Fidanci, C Un, et al.
Japanese Journal of Clinical Oncology|April 19, 2000
Multidisciplinary approach to Wilms' tumor: 18 years of experienceI Yildiz, L Yüksel, A Ozkan, et al.
Blood Cancer Journal|March 18, 2014
Deregulated WNT signaling in childhood T-cell acute lymphoblastic leukemiaO H Ng, Y Erbilgin, S Firtina, et al.
Molecular Syndromology|November 23, 2020
Clinical and Molecular Characterization of Fanconi Anemia Patients in TurkeyGüven Toksoy, Dilek Uludağ Alkaya, Gülendam Bagirova, et al.
Journal of Thrombosis and Haemostasis : JTH|February 11, 2012
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding DisordersF Peyvandi, R Palla, M Menegatti, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2NE Berber, I D Fidanci, C Un, et al.
Japanese Journal of Clinical Oncology|April 19, 2000
Multidisciplinary approach to Wilms' tumor: 18 years of experienceI Yildiz, L Yüksel, A Ozkan, et al.
Blood Cancer Journal|March 18, 2014
Deregulated WNT signaling in childhood T-cell acute lymphoblastic leukemiaO H Ng, Y Erbilgin, S Firtina, et al.
Molecular Syndromology|November 23, 2020
Clinical and Molecular Characterization of Fanconi Anemia Patients in TurkeyGüven Toksoy, Dilek Uludağ Alkaya, Gülendam Bagirova, et al.
Journal of Thrombosis and Haemostasis : JTH|February 11, 2012
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding DisordersF Peyvandi, R Palla, M Menegatti, et al.
Pageof 2