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Rare Autosomal Trisomies and Adverse Perinatal Outcomes.
Lannoo L, Van Den Bogaert K, Brison N, Dehaspe L, Dimitriadou E, Fieuws S, Melotte C, Duquenne A, Parijs I, Sznajer Y, Vancoillie L, Vandecruys H, Vermeesch JR, Devriendt K, Van Calsteren K. Lannoo L, et al. Among authors: vermeesch jr. N Engl J Med. 2024 Jul 11;391(2):184-185. doi: 10.1056/NEJMc2311046. N Engl J Med. 2024. PMID: 38986064 No abstract available.
Multiple paralogues and recombination mechanisms contribute to the high incidence of 22q11.2 Deletion Syndrome.
Vervoort L, Dierckxsens N, Sousa Santos M, Meynants S, Souche E, Cools R, Heung T, Devriendt K, Peeters H, McDonald-McGinn D, Swillen A, Breckpot J, Emanuel BS, Van Esch H, Bassett AS, Vermeesch JR. Vervoort L, et al. Among authors: vermeesch jr. Genome Res. 2024 Nov 13:gr.279331.124. doi: 10.1101/gr.279331.124. Online ahead of print. Genome Res. 2024. PMID: 39537358
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome.
Vervoort L, Dierckxsens N, Santos MS, Meynants S, Souche E, Cools R, Heung T, Devriendt K, Peeters H, McDonald-McGinn DM, Swillen A, Breckpot J, Emanuel BS, Van Esch H, Bassett AS, Vermeesch JR. Vervoort L, et al. Among authors: vermeesch jr. bioRxiv [Preprint]. 2024 Mar 18:2024.03.14.585046. doi: 10.1101/2024.03.14.585046. bioRxiv. 2024. Update in: Genome Res. 2024 Nov 13:gr.279331.124. doi: 10.1101/gr.279331.124 PMID: 38562770 Free PMC article. Updated. Preprint.
349 results