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

B van der Hagen

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 21, 2000
A correlative study of prenatal ultrasound and post-mortem findings in fetuses and infants with an abnormal karyotypeC V Isaksen, S H Eik-Nes, H G Blaas, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|January 30, 1993
[Karyotyping of fetuses with developmental disorders. A 5-year material 1985-89]J M Tuveng, S H Eik-Nes, O Sviggum, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 1, 1996
Genetics of the Berardinelli-Seip syndrome (congenital generalized lipodystrophy) in Norway: epidemiology and gene mapping. Berardinelli-Seip Study GroupT Gedde-Dahl, O Trygstad, L Van Maldergem, et al.
Acta Radiologica. Oncology|January 1, 1985
Lethal acute gamma radiation accident at Kjeller, Norway. Report of a caseP Stavem, A Brøgger, F Devik, et al.
American Journal of Human Genetics|September 1, 2000
Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15qL N Bull, E Roche, E J Song, et al.
Journal of Thrombosis and Haemostasis : JTH|September 12, 2006
Subclinical atherosclerosis and the risk of future venous thrombosis in the Cardiovascular Health StudyP B van der Hagen, A R Folsom, N S Jenny, et al.
The Journal of Pediatrics|April 25, 2003
Evidence for genetic heterogeneity in lymphedema-cholestasis syndromeMartin Frühwirth, Andreas R Janecke, Thomas Müller, et al.
American Journal of Human Genetics|February 1, 1993
Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3M H Breuning, H G Dauwerse, G Fugazza, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 21, 2000
A correlative study of prenatal ultrasound and post-mortem findings in fetuses and infants with an abnormal karyotypeC V Isaksen, S H Eik-Nes, H G Blaas, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|January 30, 1993
[Karyotyping of fetuses with developmental disorders. A 5-year material 1985-89]J M Tuveng, S H Eik-Nes, O Sviggum, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 1, 1996
Genetics of the Berardinelli-Seip syndrome (congenital generalized lipodystrophy) in Norway: epidemiology and gene mapping. Berardinelli-Seip Study GroupT Gedde-Dahl, O Trygstad, L Van Maldergem, et al.
Acta Radiologica. Oncology|January 1, 1985
Lethal acute gamma radiation accident at Kjeller, Norway. Report of a caseP Stavem, A Brøgger, F Devik, et al.
American Journal of Human Genetics|September 1, 2000
Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15qL N Bull, E Roche, E J Song, et al.
Journal of Thrombosis and Haemostasis : JTH|September 12, 2006
Subclinical atherosclerosis and the risk of future venous thrombosis in the Cardiovascular Health StudyP B van der Hagen, A R Folsom, N S Jenny, et al.
The Journal of Pediatrics|April 25, 2003
Evidence for genetic heterogeneity in lymphedema-cholestasis syndromeMartin Frühwirth, Andreas R Janecke, Thomas Müller, et al.
American Journal of Human Genetics|February 1, 1993
Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3M H Breuning, H G Dauwerse, G Fugazza, et al.
Pageof 2