1. "It's probably nothing, but…" Couples' experiences of pregnancy following an uncertain prenatal genetic result. (5th February 2020) Authors: Lou, Stina; Lomborg, Kirsten; Lewis, Celine; Riedijk, Sam; Petersen, Olav Bjørn; Vogel, Ida Journal: Acta obstetricia et gynecologica Scandinavica Issue: Volume 99:Number 6(2020) Page Start: 791 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability. Issue 12 (29th October 2013) Authors: Rasmussen, Maria; Ramsing, Mette; Petersen, Olav Bjørn; Vogel, Ida; Sunde, Lone Journal: American journal of medical genetics Issue: Volume 161:Issue 12(2013:Dec.) Page Start: 3191 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability. Issue 12 (29th October 2013) Authors: Rasmussen, Maria; Ramsing, Mette; Petersen, Olav Bjørn; Vogel, Ida; Sunde, Lone Journal: American journal of medical genetics Issue: Volume 161:Issue 12(2013:Dec.) Page Start: 3191 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A novel homozygous variant in C1QBP causes severe IUGR, edema, and cardiomyopathy in two fetuses. Issue 1 (5th March 2021) Authors: Alstrup, Morten; Vogel, Ida; Sandager, Puk; Blechingberg, Jenny; Becher, Naja; Østergaard, Elsebet Journal: JIMD reports Issue: Volume 59:Issue 1(2021) Page Start: 20 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A novel nonsense variant in MED12 associated with malformations in a female fetus. Issue 12 (22nd December 2021) Authors: Faergeman, Soren Lejsted; Becher, Naja; Andreasen, Lotte; Christiansen, Marianne; Frost, Lise; Vogel, Ida Journal: Clinical case reports Issue: Volume 9:Issue 12(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Angelman syndrome in Denmark. Birth incidence, genetic findings, and age at diagnosis. Issue 9 (2nd August 2013) Authors: Mertz, Line Granild Bie; Christensen, Rikke; Vogel, Ida; Hertz, Jens Michael; Nielsen, Karen Brøndum; Grønskov, Karen; Østergaard, John R. Journal: American journal of medical genetics Issue: Volume 161:Issue 9(2013:Sep.) Page Start: 2197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Angelman syndrome in Denmark. Birth incidence, genetic findings, and age at diagnosis. Issue 9 (2nd August 2013) Authors: Mertz, Line Granild Bie; Christensen, Rikke; Vogel, Ida; Hertz, Jens Michael; Nielsen, Karen Brøndum; Grønskov, Karen; Østergaard, John R. Journal: American journal of medical genetics Issue: Volume 161:Issue 9(2013:Sep.) Page Start: 2197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Cell-free DNA in pregnancy with choriocarcinoma and coexistent live fetus: A case report. Issue 37 (September 2016) Authors: Kristiansen, Mona Kjaerboel; Niemann, Isa; Lindegaard, Jacob Christian; Christiansen, Mette; Joergensen, Mette Warming; Vogel, Ida; Lildballe, Dorte Launholt; Sunde, Lone Other Names: Ma. Yufang section editor. Journal: Medicine Issue: Volume 95:Issue 37(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Cell-free DNA in pregnancy with choriocarcinoma and coexistent live fetus: A case report. Issue 37 (September 2016) Authors: Kristiansen, Mona Kjaerboel; Niemann, Isa; Lindegaard, Jacob Christian; Christiansen, Mette; Joergensen, Mette Warming; Vogel, Ida; Lildballe, Dorte Launholt; Sunde, Lone Editors: Ma., Yufang Journal: Medicine Issue: Volume 95:Issue 37(2016) Page Start: e4721 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Cell‐based noninvasive prenatal testing (cbNIPT) detects pathogenic copy number variations. Issue 12 (9th August 2020) Authors: Hatt, Lotte; Singh, Ripudaman; Christensen, Rikke; Ravn, Katarina; Christensen, Inga B; Jeppesen, Line Dahl; Nicolaisen, Bolette Hestbek; Kølvraa, Mathias; Schelde, Palle; Andreassen, Lotte; Farlie, Richard; Uldbjerg, Niels; Vogel, Ida Journal: Clinical case reports Issue: Volume 8:Issue 12(2020) Page Start: 2561 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗