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3q29 microduplication syndrome: New evidence for the refinement of the critical region.
Mol Genet Genomic Med. 2023 Apr;11(4):e2130. doi: 10.1002/mgg3.2130. Epub 2023 Jan 24.
Mol Genet Genomic Med. 2023.
PMID: 36691815
Free PMC article.
Rare copy number variants in ASTN2 gene in patients with neurodevelopmental disorders.
Bauleo A, Montesanto A, Pace V, Brando R, De Stefano L, Puntorieri D, Cento L, Loddo S, Calacci C, Novelli A, Falcone E.
Bauleo A, et al. Among authors: puntorieri d.
Psychiatr Genet. 2021 Dec 1;31(6):239-245. doi: 10.1097/YPG.0000000000000296.
Psychiatr Genet. 2021.
PMID: 34412080
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