Parental Decisions about Prenatal Screening and Diagnosis among Infants with Trisomy 21 in a National Cohort with High Uptake of Combined First-Trimester Screening

Autor: Miltoft, Caroline Borregaard, Wulff, Camilla B, Kjærgaard, Susanne, Ekelund, Charlotte K., Tabor, Ann, Zingenberg, Helle, Jørgensen, Finn Stener, Shalmi, Anne-Cathrine, Thagaard, Ida Näslund, Skibsted, Lillian, Hessellund, Anette, Sperling, Lene Søndergaard, Mogensen, Helle, Ibsen, Mette, Brendstrup, Lene, Petersen, Olav Bjørn, Jensen, Hanne Søndergaard, Vase, Laura, Østergaard, Marianne, Kamper, Christina H., Sørensen, Anne, Størup, Birgitte

Publikováno v: Miltoft, C B, Wulff, C B, Kjærgaard, S, Ekelund, C K, Tabor, A, Zingenberg, H, Jørgensen, F S, Shalmi, A-C, Thagaard, I N, Skibsted, L, Hessellund, A, Sperling, L S, Mogensen, H, Ibsen, M, Brendstrup, L, Petersen, O B, Jensen, H S, Vase, L, Østergaard, M, Kamper, C H, Sørensen, A, Størup, B & the Danish Fetal Medicine Study Group 2017, ' Parental Decisions about Prenatal Screening and Diagnosis among Infants with Trisomy 21 in a National Cohort with High Uptake of Combined First-Trimester Screening ', Fetal Diagnosis and Therapy, vol. 41, no. 3, pp. 209-214 . https://doi.org/10.1159/000448093

Introduction: The aim was to investigate the parental decisions about prenatal screening and diagnosis among infants with trisomy 21 (T21) in a national cohort with high uptake of combined first-trimester screening (cFTS). Material and Methods: This

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