Bart de Koning
5PUBLICATIONS
17CO-AUTHORS
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Publications (5)
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|Sep 24, 2025
Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16B.Servi J C Stevens, Wanwisa van Dijk, Nicole Y Souren
|Jun 13, 2025
Identifying a Novel Causal FAM83H Variant for Autosomal Dominant Amelogenesis Imperfecta Using Exome-Sequencing.Rick Kamps, Herm Martens, Bart de Koning
|Sep 02, 2024
Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing.Anouk E J Janssen, Rebekka M Koeck, Rick Essers
|Sep 03, 2020
Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing.Rowida Almomani, Margherita Marchi, Maurice Sopacua
|May 12, 2017
A comprehensive strategy for exome-based preconception carrier screening.Suzanne C E H Sallevelt, Bart de Koning, Radek Szklarczyk
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Frequent Collaborators
2 joint publications
Servi J C Stevens
1 joint publications
Suzanne C E H Sallevelt
1 joint publications
Christine E M de Die-Smulders
1 joint publications
Rowida Almomani
1 joint publications
Margherita Marchi
1 joint publications
Catharina G Faber
1 joint publications
Rebekka M Koeck
1 joint publications
Rick Essers
1 joint publications
Ping Cao
1 joint publications
Burcu Yaldiz
