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

R V Mikelsaar

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Hormone Research|August 31, 2000
Neonatal thyroid-stimulating hormone screening as an indirect method for the assessment of iodine deficiency in EstoniaR V Mikelsaar, M Viikmaa
Journal of Medical Genetics|May 1, 1992
Atypical case of Aarskog syndromeR V Mikelsaar, I W Lurie
Human Heredity|January 1, 1974
Dermal patterns in normal EstoniansA V Horn, R V Mikelsaar
Journal of Medical Genetics|April 1, 1996
"Pure" partial trisomy 4q25-qter owing to a de novo 4;22 translocationR V Mikelsaar, I W Lurie, T E Ilus
Journal of Medical Genetics|January 3, 2001
Mosaic terminal del(19)(q13.33:) in a girl with seizures and mental retardationR V Mikelsaar, K Varb, A Süvari, et al.
Journal of Medical Genetics|June 1, 1987
Distal trisomy 14qR V Mikelsaar, T A Ilus, I W Lurie
Journal of Medical Screening|May 12, 1998
Neonatal screening for congenital hypothyroidism in EstoniaR V Mikelsaar, R Zordania, M Viikmaa, et al.
Human Genetics|September 10, 1976
A case of trisomy for the short arm of chromosome no. 9(+9(p))M E Käosaar, A V Mikelsaar, T A Talvik, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Hormone Research|August 31, 2000
Neonatal thyroid-stimulating hormone screening as an indirect method for the assessment of iodine deficiency in EstoniaR V Mikelsaar, M Viikmaa
Journal of Medical Genetics|May 1, 1992
Atypical case of Aarskog syndromeR V Mikelsaar, I W Lurie
Human Heredity|January 1, 1974
Dermal patterns in normal EstoniansA V Horn, R V Mikelsaar
Journal of Medical Genetics|April 1, 1996
"Pure" partial trisomy 4q25-qter owing to a de novo 4;22 translocationR V Mikelsaar, I W Lurie, T E Ilus
Journal of Medical Genetics|January 3, 2001
Mosaic terminal del(19)(q13.33:) in a girl with seizures and mental retardationR V Mikelsaar, K Varb, A Süvari, et al.
Journal of Medical Genetics|June 1, 1987
Distal trisomy 14qR V Mikelsaar, T A Ilus, I W Lurie
Journal of Medical Screening|May 12, 1998
Neonatal screening for congenital hypothyroidism in EstoniaR V Mikelsaar, R Zordania, M Viikmaa, et al.
Human Genetics|September 10, 1976
A case of trisomy for the short arm of chromosome no. 9(+9(p))M E Käosaar, A V Mikelsaar, T A Talvik, et al.
Pageof 1