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American Journal of Medical Genetics. Part A|May 18, 2021
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorderCaroline Dias, Rolph Pfundt, Tjitske Kleefstra, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 8, 2022
Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up StudyCatharina J Heesterbeek, Sietse M Aukema, Robert-Jan H Galjaard, et al.NPJ Genomic Medicine|November 9, 2021
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole bloodMichael A Levy, David B Beck, Kay Metcalfe, et al.American Journal of Human Genetics|November 12, 2019
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the NetherlandsKaruna R M van der Meij, Erik A Sistermans, Merryn V E Macville, et al.Pageof 4