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Olav Bjørn Petersen

Showing results (1-10 of 79) with videos related to

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Fetal Diagnosis and Therapy|August 21, 2014
Ten years of experience with first-trimester screening for fetal aneuploidy employing biochemistry from gestational weeks 6+0 to 13+6Niels Tørring, Olav Bjørn Petersen, Niels Uldbjerg
Journal of Pregnancy|November 8, 2018
Danish Sonographers' Experiences of the Introduction of "Moderate Risk" in Prenatal Screening for Down SyndromeAnne Møller, Ida Vogel, Olav Bjørn Petersen, et al.
Journal of Genetic Counseling|May 27, 2020
How do geneticists and prospective parents interpret and negotiate an uncertain prenatal genetic result? An analysis of clinical interactionsStina Lou, Olav Bjørn Petersen, Kirsten Lomborg, et al.
Prenatal Diagnosis|March 17, 2009
Performance of first-trimester combined screening for trisomy 13 and 18 with the double test taken at a gestational age of 8 + 0 to 13 + 6Ida Kirkegaard, Olav Bjørn Petersen, Niels Uldbjerg, et al.
Prenatal Diagnosis|August 5, 2008
Improved performance of first-trimester combined screening for trisomy 21 with the double test taken before a gestational age of 10 weeksIda Kirkegaard, Olav Bjørn Petersen, Niels Uldbjerg, et al.
Ugeskrift for Laeger|October 28, 2014
[Two uncomplicated pregnancies with a univentricular heart]Tanja Østerlund Mortensen, Olav Bjørn Petersen, Keld Ejvind Sørensen
Prenatal Diagnosis|October 20, 2020
Increased prenatal detection of 22q11.2 deletion and 22q11.2 duplication after introduction of nationwide prenatal screening for trisomy 21, trisomy 13, and trisomy 18Ellen Hollands Steffensen, Jonathan Hyett, Olav Bjørn Petersen, et al.
Clinical Epidemiology|November 9, 2016
The Danish Fetal Medicine databaseCharlotte Kvist Ekelund, Tine Iskov Kopp, Ann Tabor, et al.
Gynecologic and Obstetric Investigation|September 13, 2016
Two Cases of True Uterine Artery Aneurysms Diagnosed during PregnancyJacob Mørup Schlütter, Gry Johansen, Rikke Bek Helmig, et al.
American Journal of Medical Genetics. Part A|November 21, 2013
A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variabilityMaria Rasmussen, Mette Ramsing, Olav Bjørn Petersen, et al.
Pageof 8

Showing results (1-10 of 79) with videos related to

Sort By:
Pageof 8
Fetal Diagnosis and Therapy|August 21, 2014
Ten years of experience with first-trimester screening for fetal aneuploidy employing biochemistry from gestational weeks 6+0 to 13+6Niels Tørring, Olav Bjørn Petersen, Niels Uldbjerg
Journal of Pregnancy|November 8, 2018
Danish Sonographers' Experiences of the Introduction of "Moderate Risk" in Prenatal Screening for Down SyndromeAnne Møller, Ida Vogel, Olav Bjørn Petersen, et al.
Journal of Genetic Counseling|May 27, 2020
How do geneticists and prospective parents interpret and negotiate an uncertain prenatal genetic result? An analysis of clinical interactionsStina Lou, Olav Bjørn Petersen, Kirsten Lomborg, et al.
Prenatal Diagnosis|March 17, 2009
Performance of first-trimester combined screening for trisomy 13 and 18 with the double test taken at a gestational age of 8 + 0 to 13 + 6Ida Kirkegaard, Olav Bjørn Petersen, Niels Uldbjerg, et al.
Prenatal Diagnosis|August 5, 2008
Improved performance of first-trimester combined screening for trisomy 21 with the double test taken before a gestational age of 10 weeksIda Kirkegaard, Olav Bjørn Petersen, Niels Uldbjerg, et al.
Ugeskrift for Laeger|October 28, 2014
[Two uncomplicated pregnancies with a univentricular heart]Tanja Østerlund Mortensen, Olav Bjørn Petersen, Keld Ejvind Sørensen
Prenatal Diagnosis|October 20, 2020
Increased prenatal detection of 22q11.2 deletion and 22q11.2 duplication after introduction of nationwide prenatal screening for trisomy 21, trisomy 13, and trisomy 18Ellen Hollands Steffensen, Jonathan Hyett, Olav Bjørn Petersen, et al.
Clinical Epidemiology|November 9, 2016
The Danish Fetal Medicine databaseCharlotte Kvist Ekelund, Tine Iskov Kopp, Ann Tabor, et al.
Gynecologic and Obstetric Investigation|September 13, 2016
Two Cases of True Uterine Artery Aneurysms Diagnosed during PregnancyJacob Mørup Schlütter, Gry Johansen, Rikke Bek Helmig, et al.
American Journal of Medical Genetics. Part A|November 21, 2013
A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variabilityMaria Rasmussen, Mette Ramsing, Olav Bjørn Petersen, et al.
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