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De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.
Genet Med. 2020 Mar;22(3):538-546. doi: 10.1038/s41436-019-0693-9. Epub 2019 Nov 14.
Genet Med. 2020.
PMID: 31723249
Free PMC article.
Multiple molecular diagnoses in the field of intellectual disability and congenital anomalies: 3.5% of all positive cases.
Racine C, Denommé-Pichon AS, Engel C, Tran Mau-Them F, Bruel AL, Vitobello A, Safraou H, Sorlin A, Nambot S, Delanne J, Garde A, Colin E, Moutton S, Thevenon J, Jean-Marçais N, Willems M, Geneviève D, Pinson L, Perrin L, Laffargue F, Lespinasse J, Lacaze E, Molin A, Gerard M, Lambert L, Benigni C, Patat O; Orphanomix Physician's Group; Bourgeois V, Poe C, Chevarin M, Couturier V, Garret P, Philippe C, Duffourd Y, Faivre L, Thauvin-Robinet C.
Racine C, et al.
J Med Genet. 2023 Dec 21;61(1):36-46. doi: 10.1136/jmg-2023-109170.
J Med Genet. 2023.
PMID: 37586840
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Physicochemical stability study of MYL-1401O, a biosimilar of trastuzumab, following a transient temperature excursion.
Guyader GL, Vieillard V, Paul M.
Guyader GL, et al.
J Oncol Pharm Pract. 2021 Jun;27(4):847-856. doi: 10.1177/1078155220940410. Epub 2020 Jul 13.
J Oncol Pharm Pract. 2021.
PMID: 32660375
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