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

J Leisti

Showing results (11-20 of 89) with videos related to

Pageof 9
Sort By:
The Journal of Pediatrics|June 1, 1976
Neonatal hyperglycemia and chromosome deletion (46, XX, Dq-)J Leisti, K Raivio, K Krohn
The Journal of Reproductive Medicine|May 1, 1987
Transient fetal ascites and hydrops with a favorable outcome. A report of two casesP Kirkinen, P Jouppila, J Leisti
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1971
[Intrauterine diagnosis of a chromosome translocation]P Aula, O Karjalainen, J Leisti
Prenatal Diagnosis|March 1, 1987
Early prenatal diagnosis of a lethal syndrome of multiple congenital contracturesP Kirkinen, R Herva, J Leisti
Epilepsia|August 1, 1995
Northern epilepsy syndrome: clinical course and the effect of medication on seizuresA Hirvasniemi, P Herrala, J Leisti
Neuropediatrics|December 1, 1994
Lethal arthrogryposis in Finland--a clinico-pathological study of 83 cases during thirteen yearsK Vuopala, J Leisti, R Herva
Human Genetics|May 1, 1991
Uridine enhances expression of the fragile X chromosome in human lymphocytesM Kähkönen, R Haataja, J Leisti
Human Genetics|February 1, 1994
Diagnosis of fragile X syndrome by direct mutation analysisM L Väisänen, M Kähkönen, J Leisti
Clinical Genetics|January 1, 1973
Partial trisomy 21P Aula, J Leisti, H von Koskull
American Journal of Human Genetics|September 1, 1996
Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmissionM L Väisänen, R Haataja, J Leisti
Pageof 9

Showing results (11-20 of 89) with videos related to

Sort By:
Pageof 9
The Journal of Pediatrics|June 1, 1976
Neonatal hyperglycemia and chromosome deletion (46, XX, Dq-)J Leisti, K Raivio, K Krohn
The Journal of Reproductive Medicine|May 1, 1987
Transient fetal ascites and hydrops with a favorable outcome. A report of two casesP Kirkinen, P Jouppila, J Leisti
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1971
[Intrauterine diagnosis of a chromosome translocation]P Aula, O Karjalainen, J Leisti
Prenatal Diagnosis|March 1, 1987
Early prenatal diagnosis of a lethal syndrome of multiple congenital contracturesP Kirkinen, R Herva, J Leisti
Epilepsia|August 1, 1995
Northern epilepsy syndrome: clinical course and the effect of medication on seizuresA Hirvasniemi, P Herrala, J Leisti
Neuropediatrics|December 1, 1994
Lethal arthrogryposis in Finland--a clinico-pathological study of 83 cases during thirteen yearsK Vuopala, J Leisti, R Herva
Human Genetics|May 1, 1991
Uridine enhances expression of the fragile X chromosome in human lymphocytesM Kähkönen, R Haataja, J Leisti
Human Genetics|February 1, 1994
Diagnosis of fragile X syndrome by direct mutation analysisM L Väisänen, M Kähkönen, J Leisti
Clinical Genetics|January 1, 1973
Partial trisomy 21P Aula, J Leisti, H von Koskull
American Journal of Human Genetics|September 1, 1996
Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmissionM L Väisänen, R Haataja, J Leisti
Pageof 9