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Chromosome 22q11.2 duplication is rare in a population-based cohort of Danish children with cardiovascular malformations. / Agergaard, Peter; Olesen, Charlotte; Ostergaard, John Rosendahl; Christiansen, Michael; Sørensen, Karina Meden.
Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Journal article › Research › peer-review
The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population-based study. / Agergaard, Peter; Olesen, Charlotte; Ostergaard, John Rosendahl; Christiansen, Michael; Sørensen, Karina Meden.
22q11.2 Deletion and Duplication. Cardiac and Epidemiological Aspects. / Agergaard, Peter.
Research output: Book/anthology/dissertation/report › Ph.D. thesis › Research
Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review. / Agergaard, Peter; Hebert, Anders; Sørensen, Karina M; Østergaard, John R; Olesen, Charlotte.
Children diagnosed with congenital cardiac malformations at the national university departments of pediatric cardiology: positive predictive values of data in the Danish National Patient Registry. / Agergaard, Peter; Hebert, Anders; Bjerre, Jesper; Sørensen, Karina Meden; Olesen, Charlotte; Ostergaard, John Rosendal.
Association between socio-economic factors and congenital anomalies. A population-based study among Danish women. / Olesen, Charlotte; Thrane, Nana; Agergaard, Peter; Olsen, Jørn; Henriksen, Tine Brink.