Searching for a sense of closure: parental experiences of recontacting after a terminated pregnancy for congenital malformations
Author:
Funder
Innoviris
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://www.nature.com/articles/s41431-023-01375-z.pdf
Reference31 articles.
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2. Vanakker O, Vilain C, Janssens K, Van der Aa N, Smits G, Bandelier C. et al. Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges. Eur J Med Genet [Internet]. 2014;57:151–6. https://doi.org/10.1016/j.ejmg.2014.02.002.
3. Muys J, Blaumeiser B, Jacquemyn Y, Bandelier C, Brison N, Bulk S, et al. The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations. Prenat Diagn [Internet]. 2018 ;38:1120–8. https://onlinelibrary.wiley.com/doi/full/10.1002/pd.5373.
4. Tolusso LK, Hazelton P, Wong B, Swarr DT. Beyond diagnostic yield: prenatal exome sequencing results in maternal, neonatal, and familial clinical management changes. Genet Med [Internet]. 2021;23:909–17.
5. Montaguti E, Balducci A, Perolo A, Livi A, Contro E, Casadio P, et al. Prenatal diagnosis of congenital heart defects and voluntary termination of pregnancy. Am J Obstet Gynecol MFM [Internet]. 2020;2. https://doi.org/10.1016/j.ajogmf.2020.100207.
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