17q12 deletion and duplication syndrome in Denmark-A clinical cohort of 38 patients and review of the literature von Rasmussen, Maria, Vestergaard, Else Marie, Graakjaer, Jesper, Petkov, Yanko, Bache, Iben, Fagerberg, Christina, Kibæk, Maria, Svaneby, Dea, Petersen, Olav Bjørn, Brasch-Andersen, Charlotte, Sunde, Lone

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Nuchal translucency distributions for different chromosomal anomalies in a large unselected population cohort von Christiansen, Marianne, Ekelund, Charlotte K., Petersen, Olav Bjørn, Hyett, Jon, Eastwood, Nathan, Ball, Susan, Tabor, Ann, Vogel, Ida

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Kidney anomalies diagnosed by prenatal ultrasound screening and associated non-urinary malformations: a nationwide prevalence study von Rasmussen, Maria, Olsen, Morten Smærup, Sunde, Lone, Sperling, Lene Søndergård, Petersen, Olav Bjørn

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A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability von Rasmussen, Maria, Ramsing, Mette, Petersen, Olav Bjørn, Vogel, Ida, Sunde, Lone

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Fetal Gender and Several Cytokines Are Associated with the Number of Fetal Cells in Maternal Blood - An Observational Study: e106934 von Schluetter, Jacob Moerup, Kirkegaard, Ida, Petersen, Olav Bjoern, Larsen, Nanna, Christensen, Britta, Hougaard, David M, Koelvraa, Steen, Uldbjerg, Niels

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