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Ida Vogel

Showing results (11-20 of 147) with videos related to

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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.
Sexual & Reproductive Healthcare : Official Journal of the Swedish Association of Midwives|February 22, 2021
"I had to think: This is not a child." A qualitative exploration of how women/couples articulate their relation to the fetus/child following termination of a wanted pregnancy due to Down syndromeStina Lou, Dorte Hvidtjørn, Mathilde L Jørgensen, et al.
Disability and Rehabilitation|March 29, 2023
A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women's experiences and negotiations of living with an underdeveloped uterus and vaginaAmalie Hahn Jensen, Morten Krogh Herlin, Ida Vogel, et al.
Acta Obstetricia Et Gynecologica Scandinavica|May 20, 2005
Biomarkers for the prediction of preterm deliveryIda Vogel, Poul Thorsen, Allison Curry, et al.
European Journal of Medical Genetics|January 11, 2021
Clinical and genetic evaluation of Danish patients with pycnodysostosisMia Aa Doherty, Bente L Langdahl, Ida Vogel, et al.
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.
Acta Obstetricia Et Gynecologica Scandinavica|May 15, 2023
Impact of a prenatal screening program on the Down syndrome phenotype: An interrupted time series analysisEllen Hollands Steffensen, Lars Henning Pedersen, Stina Lou, et al.
Prenatal Diagnosis|December 6, 2022
Is the first-trimester combined screening result associated with the phenotype of Down syndrome? A population-based cohort studyEllen Hollands Steffensen, Lars Henning Pedersen, Stina Lou, et al.
Acta Obstetricia Et Gynecologica Scandinavica|April 18, 2013
Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findingsElse Marie Vestergaard, Rikke Christensen, Olav B Petersen, et al.
Clinical Epidemiology|August 23, 2013
Existing data sources for clinical epidemiology: Danish registries for studies of medical genetic diseasesMary Nguyen-Nielsen, Elisabeth Svensson, Ida Vogel, et al.
Pageof 15

Showing results (11-20 of 147) with videos related to

Sort By:
Pageof 15
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.
Sexual & Reproductive Healthcare : Official Journal of the Swedish Association of Midwives|February 22, 2021
"I had to think: This is not a child." A qualitative exploration of how women/couples articulate their relation to the fetus/child following termination of a wanted pregnancy due to Down syndromeStina Lou, Dorte Hvidtjørn, Mathilde L Jørgensen, et al.
Disability and Rehabilitation|March 29, 2023
A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women's experiences and negotiations of living with an underdeveloped uterus and vaginaAmalie Hahn Jensen, Morten Krogh Herlin, Ida Vogel, et al.
Acta Obstetricia Et Gynecologica Scandinavica|May 20, 2005
Biomarkers for the prediction of preterm deliveryIda Vogel, Poul Thorsen, Allison Curry, et al.
European Journal of Medical Genetics|January 11, 2021
Clinical and genetic evaluation of Danish patients with pycnodysostosisMia Aa Doherty, Bente L Langdahl, Ida Vogel, et al.
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.
Acta Obstetricia Et Gynecologica Scandinavica|May 15, 2023
Impact of a prenatal screening program on the Down syndrome phenotype: An interrupted time series analysisEllen Hollands Steffensen, Lars Henning Pedersen, Stina Lou, et al.
Prenatal Diagnosis|December 6, 2022
Is the first-trimester combined screening result associated with the phenotype of Down syndrome? A population-based cohort studyEllen Hollands Steffensen, Lars Henning Pedersen, Stina Lou, et al.
Acta Obstetricia Et Gynecologica Scandinavica|April 18, 2013
Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findingsElse Marie Vestergaard, Rikke Christensen, Olav B Petersen, et al.
Clinical Epidemiology|August 23, 2013
Existing data sources for clinical epidemiology: Danish registries for studies of medical genetic diseasesMary Nguyen-Nielsen, Elisabeth Svensson, Ida Vogel, et al.
Pageof 15