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 Maríková

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
Casopis Lekaru Ceskych|January 10, 1986
[Further development of the MYOPAT knowledge base for the differential diagnosis of progressive muscular dystrophy]T Maríková, E Seemanová, H Krautwurmová
Ceskoslovenska Pediatrie|August 1, 1990
[Genetics in epilepsy]T Maríková, M Lehovský, J Kraus
Ceskoslovenska Pediatrie|November 1, 1987
[Use of expert systems in the clinical genetics of polydactyly and progressive muscular dystrophies]T Maríková, E Seemanová, I Hrycejová, et al.
Casopis Lekaru Ceskych|January 25, 1985
[Differential diagnosis of progressive muscular dystrophies using an expert computer system]T Maríková, E Seemanová, V Marík, et al.
Ceskoslovenska Pediatrie|November 1, 1987
[The fragile X chromosome syndrome]E Seemanová, A Schmidt, I Subrt, et al.
Casopis Lekaru Ceskych|December 4, 1996
[A method for detection of germinal mutations in the p53 tumor suppressor gene]Z Sedlácek, V Kríz, E Seemanová, et al.
Casopis Lekaru Ceskych|July 31, 1996
[Amplification of oncogenes in solid tumors in children]J Mares, V Lesková, Z Sedlácek, et al.
Casopis Lekaru Ceskych|February 18, 1983
[Macro-orchism. A significant symptom in the detection of the fragile X chromosome syndrome]E Seemanová, A Schmidt, K Popelová, et al.
Casopis Lekaru Ceskych|December 9, 2004
[Case reports of patients with a marker chromosome]E Kocárek, D Novotná, T Maríková, et al.
Neoplasma|August 26, 1998
Oncogene amplification and expression in pediatric solid tumorsJ Mares, V Polanská, H Görgens, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Casopis Lekaru Ceskych|January 10, 1986
[Further development of the MYOPAT knowledge base for the differential diagnosis of progressive muscular dystrophy]T Maríková, E Seemanová, H Krautwurmová
Ceskoslovenska Pediatrie|August 1, 1990
[Genetics in epilepsy]T Maríková, M Lehovský, J Kraus
Ceskoslovenska Pediatrie|November 1, 1987
[Use of expert systems in the clinical genetics of polydactyly and progressive muscular dystrophies]T Maríková, E Seemanová, I Hrycejová, et al.
Casopis Lekaru Ceskych|January 25, 1985
[Differential diagnosis of progressive muscular dystrophies using an expert computer system]T Maríková, E Seemanová, V Marík, et al.
Ceskoslovenska Pediatrie|November 1, 1987
[The fragile X chromosome syndrome]E Seemanová, A Schmidt, I Subrt, et al.
Casopis Lekaru Ceskych|December 4, 1996
[A method for detection of germinal mutations in the p53 tumor suppressor gene]Z Sedlácek, V Kríz, E Seemanová, et al.
Casopis Lekaru Ceskych|July 31, 1996
[Amplification of oncogenes in solid tumors in children]J Mares, V Lesková, Z Sedlácek, et al.
Casopis Lekaru Ceskych|February 18, 1983
[Macro-orchism. A significant symptom in the detection of the fragile X chromosome syndrome]E Seemanová, A Schmidt, K Popelová, et al.
Casopis Lekaru Ceskych|December 9, 2004
[Case reports of patients with a marker chromosome]E Kocárek, D Novotná, T Maríková, et al.
Neoplasma|August 26, 1998
Oncogene amplification and expression in pediatric solid tumorsJ Mares, V Polanská, H Görgens, et al.
Pageof 1