Malgorzata Srebniak - Dissemin

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All papers authored by Malgorzata Srebniak

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2021 Maurike Groot‐van der Mooren

ORCID

ORCID

, Michel E. Weijerman, Mariette J. V. Hoffer, Jeroen Knijnenburg, Anne‐Marie M. F. Kevie‐Kersemaekers, Angelique J. A. Kooper, Els Voorhoeve, Birgit Sikkema‐Raddatz, Laura J. C. M. Zutven, Malgorzata Ilona Srebniak

ORCID

, Karin Huijsdens‐van Amsterdam, John J. M. Engelen, Dominique Smeets, Anton H. Kaam and 1 other authors

Does non‐invasive prenatal testing affect the livebirth prevalence of Down syndrome in the Netherlands? A population‐based register study

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2020 Karin E. M. Diderich, Marjon A. van Slegtenhorst, Yolande van Bever, Ingrid M. B. H. van de Laar, Kathleen Romijn, Marieke Joosten, Lutgarde C. P. Govaerts, Marike Polak

ORCID

, Hennie T. Bruggenwirth, Martina Wilke, Marjon A. Slegtenhorst, Yolande Bever, Alice S. Brooks, Grazia M. S. Mancini, Ingrid M. B. H. Laar and 7 other authors

The potential diagnostic yield of whole exome sequencing in pregnancies complicated by fetal ultrasound anomalies

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2019 Malgorzata I. Srebniak

ORCID

, Maarten F. C. M. Knapen, Lutgarde C. P. Govaerts, Marike Polak

ORCID

, Marieke Joosten, Karin E. M. Diderich, Laura J. C. M. van Zutven, Krista A. K. E. Prinsen, Sam Riedijk, Attie T. J. I. Go, Robert‐Jan H. Galjaard, Lies H. Hoefsloot, Diane Van Opstal

Social and medical need for whole genome high resolution NIPT

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2018 M. I. Srebniak

ORCID

, M. Joosten, M. F. C. M. Knapen, L. R. Arends, M. Polak

ORCID

, S. van Veen, A. T. J. I. Go, D. Van Opstal

Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta-analysis

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This paper was not found in any repository, but could be made available legally by the author.

2017 Malgorzata I. Srebniak

ORCID

, Maarten F. C. M. Knapen, Marike Polak

ORCID

, Marieke Joosten, Karin E. M. Diderich, Lutgarde C. P. Govaerts, Marjan Boter, Joan N. R. Kromosoeto, Daniella Aloysia C. M. van Hassel, Gido Huijbregts, Wilfred F. J. van IJcken, Roger Heydanus, Anneke Dijkman, Toon Toolenaar, Femke A. T. de Vries and 4 other authors

The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies

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